Relevant bibliographies by topics / Perceptions of patient / family

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Perceptions of patient / family'

Author: Grafiati
Published: 11 September 2021
Last updated: 1 February 2022

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Journal articles on the topic "Perceptions of patient / family"

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Hardin, Sally B., Rose Magee, Mary Hite Vinson, Marilyn Owen, Elizabeth Hyatt, and Diane Stratmann. "Patient and Family Perceptions of Restraints." Journal of Holistic Nursing 11, no. 4 (1993): 383–97. http://dx.doi.org/10.1177/089801019301100407.

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LIAW, S. TENG. "Patient and General Practitioner Perceptions of Patient-held Health Records." Family Practice 10, no. 4 (1993): 406–15. http://dx.doi.org/10.1093/fampra/10.4.406.

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Blumenthal, Karen J., Alyna T. Chien, and Sara J. Singer. "Relationship among team dynamics, care coordination and perception of safety culture in primary care." Family Practice 35, no. 6 (2018): 718–23. http://dx.doi.org/10.1093/fampra/cmy029.

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Abstract Background There remains a need to improve patient safety in primary care settings. Studies have demonstrated that creating high-performing teams can improve patient safety and encourage a safety culture within hospital settings, but little is known about this relationship in primary care. Objective To examine how team dynamics relate to perceptions of safety culture in primary care and whether care coordination plays an intermediating role. Research Design This is a cross-sectional survey study with 63% response (n = 1082). Subjects The study participants were attending clinicians, resident physicians and other staff who interacted with patients from 19 primary care practices affiliated with Harvard Medical School. Main Measures Three domains corresponding with our main measures: team dynamics, care coordination and safety culture. All items were measured on a 5-point Likert scale. We used linear regression clustered by practice site to assess the relationship between team dynamics and perceptions of safety culture. We also performed a mediation analysis to determine the extent to which care coordination explains the relationship between perceptions of team dynamics and of safety culture. Results For every 1-point increase in overall team dynamics, there was a 0.76-point increase in perception of safety culture [95% confidence interval (CI) 0.70–0.82, P < 0.001]. Care coordination mediated the relationship between team dynamics and the perception of safety culture. Conclusion Our findings suggest there is a relationship between team dynamics, care coordination and perceptions of patient safety in a primary care setting. To make patients safer, we may need to pay more attention to how primary care providers work together to coordinate care.
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McLennan, Marianne, Gina Starko Anderson, and Kerrie Pain. "Rehabilitation learning needs: patient and family perceptions." Patient Education and Counseling 27, no. 2 (1996): 191–99. http://dx.doi.org/10.1016/0738-3991(95)00799-7.

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Golembeski, Susan, Beth Willmitch, and Sandy S. Kim. "Perceptions of the Care Experience in Critical Care Units Enhanced by a Tele-ICU." AACN Advanced Critical Care 23, no. 3 (2012): 323–29. http://dx.doi.org/10.4037/nci.0b013e31825ed8bb.

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The purpose of this study was to determine patients’ and families’ perceptions of care in 10 critical care units enhanced by a tele–intensive care unit (ICU) in a 5-hospital health care system. Patients and family members who had a critical care experience were approached for participation. An adapted version of the Schmidt Perception of Nursing Care Survey was administered. The Schmidt Perception of Nursing Care Survey factors–-seeing the individual patient, explaining, responding, and watching over—were analyzed for 637 participants (263 before and 374 after the tele-ICU implementation). Analysis of data from patients and family members indicated significantly higher means for the following factors: seeing the individual patient (P =.004), responding (P =.002), and watching over (P =.006) only when there was an awareness by the patient and family members that the care team was at the bedside and at the tele-ICU command center. The perceptions of care in these cases may suggest an improved patient experience when a tele-ICU is part of the care team.
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Anderson, Marguerite “Peggy”, and Eira Kristiina Hyrkas. "Patient and family perceptions of an inpatient journal." Nursing 51, no. 7 (2021): 62–68. http://dx.doi.org/10.1097/01.nurse.0000754044.26660.0b.

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Okado, Izumi, Ian Pagano, Tracey Hewitt, et al. "Perceptions of cancer care coordination in patient-family caregiver dyads." Journal of Clinical Oncology 38, no. 15_suppl (2020): e14036-e14036. http://dx.doi.org/10.1200/jco.2020.38.15_suppl.e14036.

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e14036 Background: Family caregivers (FCGs) can play a key role in coordinating care for cancer patients. However, little is known about FCGs’ perspectives of care coordination (CC). In this cross-sectional study, we evaluated perceptions of CC in cancer patient-family caregiver dyads using the Care Coordination Instrument (CCI), a validated self-report measure with excellent psychometric properties. Methods: Patients receiving active treatment for cancer and their primary FCGs ( N = 54 dyads) completed the 29-item CCI (patient) and the CCICG (a parallel FCG version) at private oncology practices or hospital-based facilities from June to Sept. 2019. The CCI and CCICG assess overall perceptions of CC (Total) and across 3 domains: Communication, Navigation, and Operational. The CCICG includes a supplemental questionnaire that assesses the degree of caregiver CC involvement on a 4-point Likert scale. Mixed regression models were used to examine differences between patients and FCGs’ perceptions of CC and to identify predictors of dyadic differences on the CCI scores. Pearson’s correlation was used to evaluate associations between FCGs’ perceptions of CC and the degree of caregiver involvement. Results: CCICG Total scores demonstrated a bimodal distribution, representing FCGs’ perceptions of CC in distinct high and low subgroups; thus, all analyses were conducted by subgroups (highCG, lowCG). Overall, no dyadic differences were found in the highCG group on the CCI scores. However, in the lowCG group, FCGs reported poorer Total ( p < .01), Communication ( p < .01), Navigation ( p < .01), and Operational ( p < .05) scores than patients. Provider setting (private practices) and the absence of an identified patient navigator significantly predicted poorer FCG Total scores compared to patients’ perceptions ( p < .05). FCGs’ Total scores were inversely associated with the degree of caregiver involvement among FCGs in the lowCG group ( p < .05) but not among FCGs in the highCG group. Conclusions: Our findings demonstrate that a subgroup of FCGs has poorer perceptions of CC that differ significantly from patient perceptions and is most apparent for patients receiving treatment in a private practice setting and in the absence of a patient navigator. These FCGs report a high degree of caregiver involvement and may be providing additional CC support that is not recognized by cancer patients. These findings underscore the need for interventions to support FCG CC involvement as a member of the care team in order to improve the quality and value of patient-centered cancer care delivery.
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HOLLOWAY, RICHARD L., JOHN C. ROGERS, and SUSAN L. GERSHENHORN. "Differences Between Patient and Physician Perceptions of Predicted Compliance." Family Practice 9, no. 3 (1992): 318–22. http://dx.doi.org/10.1093/fampra/9.3.318.

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Maskell, Katherine, Paula McDonald, and Priyamvada Paudyal. "The usefulness of health education materials in GP waiting rooms: a cross-sectional study." British Journal of General Practice 68, suppl 1 (2018): bjgp18X696845. http://dx.doi.org/10.3399/bjgp18x696845.

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BackgroundMore than half of patients in the UK wait between 5 and 15 minutes before seeing the GP, and this time in the waiting room (WR) provides an ideal opportunity for patient education.AimTo assess patients’ perceptions of the usefulness, noticeability and attractiveness of health education materials (HEMs); and the variety, number, topics, design and accessibility of these HEMs.MethodAn anonymous questionnaire was distributed to patients in the WR to assess their use of health information and perceptions of HEMs. A survey measured the availability of HEMs in the WR and evaluated their quality against 16 accessibility and design criteria.ResultsA total of 556 questionnaires were completed (response rate 97.9%). On average, WRs contained 72 posters covering 23 topics, and 53 leaflets covering 24 topics. Multivariate analysis showed that patients’ perception of usefulness was significantly associated with reading in the WR, using written HEMs, and not having a university degree; whilst noticeability was associated with reading in the WR, and being female. Attractiveness was associated with not having a university degree and shorter waiting time.ConclusionThis study suggests that a wide variety of HEMs are available, and that many patients find them useful and noticeable, however, fewer find them well-designed and attractive. Future research should focus on the effectiveness of generally available HEMs at changing knowledge, attitudes, intentions, and behaviours; and utilising technology to deliver innovative means of providing patient health information.
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Fisher, MaryDee, Donna Weyant, Susan Sterrett, Heather Ambrose, and Abraham Apfel. "Perceptions of interprofessional collaborative practice and patient/family satisfaction." Journal of Interprofessional Education & Practice 8 (September 2017): 95–102. http://dx.doi.org/10.1016/j.xjep.2017.07.004.

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Dissertations / Theses on the topic "Perceptions of patient / family"

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Janes, Laurie Ann. "Emergency nurses' perceptions of their role as patient and family teachers." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp05/mq24858.pdf.

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Smith, Cheryl. "Patients’ Perceptions of Patient-Centered Care and the Hospital Experience Pre- and Post-Discharge." Digital Commons @ East Tennessee State University, 2018. https://dc.etsu.edu/etd/3388.

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Florence Nightingale used the principles of patient-centered care as the foundation for nursing practice. Today, patient-centered care delivery is part of the healthcare reform process that extends interprofessionally throughout all settings of healthcare in the United States (U.S.). Patient satisfaction measurement is one primary determinant of effective patient-centered care. The standardized Hospital Consumer Assessment of Healthcare Providers and Systems (HCAHPS) survey and methods is a nation-wide tool used to measure patient satisfaction. However, this method of patient satisfaction assessment relies on recollections of patients’ hospital experiences and requires accurate memory and recall. This study sought to examine the effect of the memory-experience gap on patients’ perceptions of their hospital experiences and address this research question: Are there any statistical differences between in-hospital and two-week post-discharge perceptions of patient-centered care as measured with HCAHPS patient satisfaction ratings on (a) the composite scores for communication with nurses, communication with physicians, communication about medicines, pain management, staff responsiveness, (b) the individual scores for the hospital environment’s cleanliness and quietness, and the inclusion of patient and family preferences in the plan of care, and (c) the overall global rating score? The design was a non-experimental, prospective, descriptive correlational study. The setting was a 255-bed regional hospital that serves individuals from eight surrounding rural counties in southern middle Tennessee. The case-mix contained diverse individuals with multiple economic, environmental, physical, social and spiritual dynamics. A convenience sample of 82 adult patients ages 26 - 93 represented mainly Caucasian females with mostly cardiovascular and respiratory illnesses who had a minimum one-day stay.
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Sisson, Rebecca. "Assessing and Addressing Family Members' Attitudes and Perceptions of Acute Necrotizing Encephalopathy." University of Cincinnati / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1337887857.

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Dumit, Nuhad Yazbik. "Perceptions of cardiac self-care among Lebanese patients and their family caregivers /." Connect to full text via ProQuest. Limited to UCD Anschutz Medical Campus, 2008.

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Thesis (Ph.D. in Nursing) -- University of Colorado Denver, 2008.
Typescript. Includes bibliographical references (leaves 194-203). Free to UCD Anschutz Medical Campus. Online version available via ProQuest Digital Dissertations;
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Naidoo, Melissa. "Family and patient perception of physiotherapy care rendered to patients in the cardiothoracic intensive care unit." University of the Western Cape, 2018. http://hdl.handle.net/11394/6978.

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Magister Artium - MA
Background: Physiotherapists are involved in the management of patients in the cardiothoracic Intensive Care Unit (ICU). Patient and family perception of care has become an important measure in evaluating the quality of care, including care in the intensive care setting. Overall Aim: To explore and describe the family and patient perception of physiotherapy care rendered in a public sector cardiothoracic ICU in the Western Cape, South Africa. Method: This study was conducted in two phases. Phase 1 (scoping review) identified and described available outcomes for measuring family perception of ICU care by searching six databases from inception to the 20th June 2018. Results from the scoping review informed the discussion schedule for the first primary study of Phase 2. Phase 2 (two exploratory descriptive qualitative primary studies) explored and described i) family perception and ii) patient perception of physiotherapy care in a cardiothoracic ICU. Audio-taped, individual face to face semi-structured interviews were conducted with family and patient participants that met the inclusion and exclusion sampling criteria (purposive sampling). Data was transcribed verbatim and analysed using deductive-inductive thematic content analysis. The data was coded, categorised and themes were generated. Trustworthiness of the data was ensured through methods addressing credibility, dependability, confirmability and transferability. Results: A total of ten full text studies were included in the scoping review. Included studies were published between 2006 and 2017, were conducted in both developed and developing countries, in different ICUs (except cardiothoracic ICU)and all used different quantitative outcome measures to measure family perception of ICU care. Thirteen cardiothoracic ICU patients and their respective family members partook in the studies describing patient and family perception of cardiothoracic ICU physiotherapy care. The median patient age was 62 years; the mean ICU length of stay 6 days and the median family age was 55. Themes arising from the family perception of care data analysed included: i) understanding of physiotherapy care (the role of the physiotherapist, perceived benefit of physiotherapy and communication), family involvement in physiotherapy care (physical presence during physiotherapy sessions and decision-making), and satisfaction of physiotherapy ICU care. Themes arising from patient perception of care data analysed included: i) Physiotherapy management of patients, ii) The Physiotherapists – skill, iii) knowledge and professionalism, iv) Continuity of Care, v) Tangibility, vi) Physiotherapy benefits, vii) Decision-Making, viii) Communication, ix) Satisfaction of Physiotherapy ICU care. Overall, family and patients were satisfied with the physiotherapy care in the cardiothoracic ICU. However, there were areas of improvement such as the understanding of physiotherapy care, communication, family involvement in the physiotherapy care and decision-making. Conclusion: While there are multiple quantitative measures for measuring family perception of ICU care there is no “gold” standard measure that has been identified. A qualitative measure and research design would allow richer in-depth information on family perception of ICU care. The findings from the family and patient perception of cardiothoracic ICU physiotherapy care are influenced by many factors. While family and patients perceive cardiothoracic ICU physiotherapy care both positively and negatively, the majority of patient and family were satisfied overall with the care the patient received. Family perception of ICU physiotherapy care should be evaluated in order to identify areas for improvement in quality of care and could add to the body of evidence in ICU physiotherapy practice.
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Davis, Linda 1951. "Perceptions of families and nurses regarding family involvement in the care of the elderly, long term care patient." Thesis, McGill University, 1989. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=55674.

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Garlington, Jennifer Erin, and Jennifer Erin Garlington. "Exploring Family Perceptions About Primary Care Management Following Diagnosis of Type 1 Diabetes in Preschool-Age Children." Diss., The University of Arizona, 2016. http://hdl.handle.net/10150/621004.

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Purpose: To describe family perceptions about pediatric primary care management following diagnosis of type 1 diabetes mellitus (T1DM) in preschool-aged children living in the Pacific Northwest region of the United States. Study Design and Method: Mothers of children diagnosed with T1DM before the fifth birthday and within the past two years were recruited anonymously through two regional support groups. Perceptions about pediatric primary care management following T1DM diagnosis were elicited through an anonymous 30-item online survey. Demographic characteristics of mother and child were obtained as well as information about five important domains of health care management for a young child with T1DM: (1) multidisciplinary, (2) holistic and compassionate, (3) accessible and communicative, (4) uses current standards and technology, and (5) actively promotes safe self-management. Results: Twenty-one biological mothers participated in this study, each on behalf of a child diagnosed with T1DM who fit inclusion criteria. Overall mothers held positive perceptions about care management by PCPs and endocrinologists within context of each of the five domains. Most mothers felt included in care planning, valued periodic well-child exams, and believed the child's providers were accessible, communicated effectively, and usually demonstrated consideration/compassion for the family. Although a majority of mothers at least somewhat agreed that the PCP used current standards and technology to care for the child, and functioned as the center of his/her health care coordination, these domains elicited a slightly greater number of responses indicating uncertainty or disagreement. Clinical Implications: Nurses and pediatric practitioners can use findings from this study to plan continued exploration into the perceptions and care management needs of families following diagnosis of a very young child with T1DM. The domains of care used to assess mothers' perceptions about care management-based on tenets of the Chronic Care Model (CCM) and Patient Centered Medical Home (PCMH)-can be used by pediatric PCPs and endocrinologists to dialogue with patients and staff about how care management may be improved for these families. Providing opportunities for feedback to the families of young children with T1DM should be encouraged so future research can examine relationships between care management variables and clinical outcomes.
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Eaton, Bill. "Symptoms of patients hospitalized because of malignancy : a comparison of the perceptions of the patient, the next of kin, and the nurse /." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape9/PQDD_0005/MQ42371.pdf.

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Davis, Nancy Lynn. "Perceptions of spouses of head injured survivors." Thesis, The University of Arizona, 1989. http://hdl.handle.net/10150/277111.

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This exploratory study was designed to discover the culture of living with a head injured spouse. Using the ethnographic approach, five spouses of head injured survivors were interviewed. Analysis of data yielded five domains of meaning: concerns as a result of role transition, social isolation, loss, future and coping. Two cultural themes emerged as "no one understands" and a "wish list." Implications for nursing practice include increasing awareness of health care professionals regarding perceptions and needs of spouses of head injured survivors.
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Warner, Judy A. "Perceptions of family caregivers of non-institutionalized Alzheimer's patients about support groups." Virtual Press, 1999. http://liblink.bsu.edu/uhtbin/catkey/1133742.

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The purpose of this descriptive study was to document and analyze the perceptions of family caregivers of non-institutionalized Alzheimer's patients about the benefits and limitations of Alzheimer's support groups. Survey methodology was used to survey caregivers and support group leaders from eight Alzheimer's support groups in the central Indiana area. Several of the major findings challenge the literature. These findings are as follows: The majority of caregivers attended the support group to receive information. None of the caregivers attended the support group due to frustration, and only one caregiver responded that relieving frustration was a benefit of participating in the support group. A majority of caregivers and support group leaders were positive about mixed (spouses and adult children) support groups. A majority of caregivers responded that they did not have guilt, anger, fears about caregiving in the future, or stress concerning their caregiving responsibilities. The study generated several implications that can be used by planners to improve support groups.
Department of Educational Leadership
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Books on the topic "Perceptions of patient / family"

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Magee, Seamus. Patients' perceptions and experiences of services provided by family doctors: Joint report by Southern Health and Social Services Council and Southern Health and Social Services Board. Southern Health and Social Services Council, 1995.

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Leventhal, Amy. Relocation of public hospital patients: Perceptions of patient representatives. Gerontology Institute and Center, University of Massachusetts/Boston, 1992.

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Tom, O'Connor. Bridging the gap: Practising nurses' perceptions of patient advocacy. The Author), 2002.

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Devinsky, Orrin. Epilepsy: Patient and family guide. 3rd ed. Demos Medical Pub., 2008.

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Devinsky, Orrin. Epilepsy: Patient and family guide. 2nd ed. F.A. Davis Co., 2002.

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Andrew, Treacher, and White Carolyn, eds. Introducing user-friendly family therapy. Routledge, 1995.

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Meehl, Brian. Out of Patience. Yearling, 2008.

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Zastocki, Deborah K. Home care: Patient and family instructions. W.B. Saunders Co., 1989.

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Murtagh, John. Patient education. 2nd ed. McGraw-Hill, 1996.

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Scanlon, Adrian. Psychiatric nurses perceptions of the constituents of the therapeutic relationship. Nova Science, 2009.

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Book chapters on the topic "Perceptions of patient / family"

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Tompson, Martha C., and Amy G. Weisman. "Examining Patients’ Perceptions of their Relatives’ Expressed Emotion." In New Family Interventions and Associated Research in Psychiatric Disorders. Springer Vienna, 2002. http://dx.doi.org/10.1007/978-3-7091-6148-7_4.

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Tunzi, Marc, and George Saba. "Suicidal Patient." In Family Medicine. Springer New York, 1998. http://dx.doi.org/10.1007/978-1-4757-2947-4_33.

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Galchutt, Paul, and Judy Connolly. "Palliative Chaplain Spiritual Assessment Progress Notes." In Charting Spiritual Care. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-47070-8_11.

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Abstract Research question “What is helpful as well as missing from palliative chaplain spiritual assessment progress notes?” arose from the context of seeking to know how palliative chaplain spiritual assessment progress notes can best be relevant and make a difference for a patient’s care. Seven focus groups, two of which were in a children’s hospital context, were hosted with 42 non-chaplain palliative team participants. The major results revealed four important considerations for palliative care chaplains. First, palliative interprofessional team members want more help and information regarding a patient’s decision-making, especially related to a patient’s religion and/or spirituality. Second, and in line with palliative care principles, the participants discussed their desire for relevant notation on a patient’s sense of suffering and coping. Third, a request was made for the chaplain to consistently document his/her perception of emotion emerging from the patient and/or family. The last major result to emerge was that the progress notes should have a summary content section at the top of the note with the most important information contained there.
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Tunzi, Marc, and George Saba. "The Suicidal Patient." In Family Medicine. Springer New York, 2003. http://dx.doi.org/10.1007/978-0-387-21744-4_33.

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Hartmann, Peter M. "The Suicidal Patient." In Family Medicine. Springer New York, 1994. http://dx.doi.org/10.1007/978-1-4757-4005-9_29.

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Shipley, Sonya R., Molly S. Clark, and David R. Norris. "The Suicidal Patient." In Family Medicine. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-1-4939-0779-3_34-1.

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Shipley, Sonya R., Molly S. Clark, and David R. Norris. "The Suicidal Patient." In Family Medicine. Springer New York, 2020. http://dx.doi.org/10.1007/978-1-4939-0779-3_34-2.

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Shipley, Sonya R., Molly S. Clark, and David R. Norris. "The Suicidal Patient." In Family Medicine. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-04414-9_34.

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Emery-Tiburcio, Erin E., and Victoria L. Webb. "Patient-Family Education." In Encyclopedia of Clinical Neuropsychology. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-57111-9_418.

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Emery, Erin E. "Patient-Family Education." In Encyclopedia of Clinical Neuropsychology. Springer New York, 2011. http://dx.doi.org/10.1007/978-0-387-79948-3_418.

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Conference papers on the topic "Perceptions of patient / family"

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Kozhyna, Hanna, Kateryna Zelenska, and Olha Kaploukh. "GENDER FEATURES OF THE PERCEPTION OF THE DISEASE BY THE FAMILY OF A PATIENT WITH DEMENTIA." In TENDENZE ATTUALI DELLA MODERNA RICERCA SCIENTIFICA. European Scientific Platform, 2020. http://dx.doi.org/10.36074/05.06.2020.v3.09.

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Proctor, Cecile J., Danie A. Beaulieu, Anthony J. Reiman, and Lisa A. Best. "LIVING WELL AFTER CANCER: THE IMPACT OF SOCIAL SUPPORT AND PRODUCTIVE LEISURE." In International Psychological Applications Conference and Trends. inScience Press, 2021. http://dx.doi.org/10.36315/2021inpact029.

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"It is now recognized that the ""cancer experience"" extends beyond diagnosis, treatment, and end-of-life care. Relative to individuals who have not faced a cancer diagnosis, cancer survivors report increased mental health concerns and lowered physical and psychological well-being (Langeveld et al., 2004). Health-related quality of life encompasses overall physical (e.g., energy, fatigue, pain, etc.) and psychological functioning (e.g., emotional well-being, etc.), as well as general health perceptions (Hays & Morales, 2001). Nayak and colleagues (2017) reported that 82.3% of cancer patients had below-average quality of life scores, with the lowest scores found in the general, physical, and psychological well-being domains. Research suggests that various positive lifestyle variables, including social connectedness, leisure activity, and mindfulness practices are associated with increased quality of life in cancer patients (Courtens et al., 1996; Fangel et al., 2013; Garland et al., 2017). In this study, 350 cancer survivors completed an online questionnaire package that included a detailed demographic questionnaire with medical and online support and leisure activity questions. Additional measures were included to assess quality of life (QLQ-C30; Aaronson et al., 1993), social connectedness (Social and Emotional Loneliness Scale for Adults, SELSA-S; DiTommaso et al., 2004), and mindfulness (Adolescent and Adult Mindfulness Scale, AAMS; Droutman et al., 2018). Results show that increased QOL is predicted by increased medical support, lower family loneliness, self-acceptance, and engaging in a variety of leisure activities. Encouraging family support, including the patient in the decision-making process, encouraging a variety of physically possible leisure activities, and normalizing negative emotions surrounding diagnosis and disease symptoms are all ways that overall QoL can be improved."
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Sibona, Christopher, Jon Brickey, Steven Walczak, and Madhavan Parthasarathy. "Patient Perceptions of Electronic Medical Records." In 2010 43rd Hawaii International Conference on System Sciences. IEEE, 2010. http://dx.doi.org/10.1109/hicss.2010.302.

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Ross, M. K., S. Friedman, I. Radparvar, and G. Ryan. "Parental Perceptions of Patient Reported Outcome Measures and the Patient Portal." In American Thoracic Society 2021 International Conference, May 14-19, 2021 - San Diego, CA. American Thoracic Society, 2021. http://dx.doi.org/10.1164/ajrccm-conference.2021.203.1_meetingabstracts.a3475.

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Suhartanto, Paulus Eddy, Markus Hartono, and Frikson Sinambela. "Perceptions of Communication Organizational - Family and Authentic Leadership." In International Conference on Psychological Studies (ICPSYCHE 2020). Atlantis Press, 2021. http://dx.doi.org/10.2991/assehr.k.210423.051.

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Dudnikova, Tatyana. "Family Perceptions Of People With Different Typology Of Individuality." In ICEEPSY 2019 - 10th International Conference on Education and Educational Psychology. Cognitive-Crcs, 2019. http://dx.doi.org/10.15405/epsbs.2019.11.66.

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HUANG, Chih-Hsuan, Li-Xin ZENG, Hsin-Hung WU, Yii-Ching LEE, and Li LI. "Promoting Patient-oriented Medical Services: The Perceptions of Nurses toward Patient Safety Culture." In 2018 5th International Conference on Management Science and Management Innovation (MSMI 2018). Atlantis Press, 2018. http://dx.doi.org/10.2991/msmi-18.2018.24.

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PETERS, UWE HENRIK. "THE FAMILY OF THE DEPRESSIVE PATIENT: FROM MELANCHOLIC TYPE OF MELANCHOLIC FAMILY." In IX World Congress of Psychiatry. WORLD SCIENTIFIC, 1994. http://dx.doi.org/10.1142/9789814440912_0081.

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Ripka, Irina, and Larysa Klymanska. "Formation of the Child's Perceptions of his Own Family in the Process of Family Education." In SOCIOLOGY – SOCIAL WORK AND SOCIAL WELFARE – REGULATION OF SOCIAL PROBLEMS. NDSAN (MFC - coordinator of the NDSAN), 2020. http://dx.doi.org/10.32437/sswswproceedings-2020.irlk.

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Little, EM, S. Grevich, JL Huber, et al. "THU0537 Family and patient's perception of dietary intervention in juvenile idiopathic arthritis (JIA)." In Annual European Congress of Rheumatology, 14–17 June, 2017. BMJ Publishing Group Ltd and European League Against Rheumatism, 2017. http://dx.doi.org/10.1136/annrheumdis-2017-eular.2330.

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Reports on the topic "Perceptions of patient / family"

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Grant, Shannon. Fatigue Impacting Patient Safety: Literature Review and Local Perceptions. Defense Technical Information Center, 2006. http://dx.doi.org/10.21236/ada499202.

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Bennett, Wendy L., Samantha Pitts, Hanan Aboumatar, et al. Strategies for Patient, Family, and Caregiver Engagement. Agency for Healthcare Research and Quality (AHRQ), 2020. http://dx.doi.org/10.23970/ahrqepctb36.

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Abramson, Lisa. The relationship of patients' perceptions of physicians' communication style to patient satisfaction. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.6004.

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Landrigan, Christopher, Alisa Khan, and Matthew Ramotar. Does a Patient- and Family-Centered Hospital Communications Program Reduce Medical Errors? Patient-Centered Outcomes Research Institute® (PCORI), 2019. http://dx.doi.org/10.25302/8.2019.cdr.130603556.

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Ki, Young, Fitri Putjuk, Endang Basuki, and Adrienne Kols. Increasing client participation in family planning consultations: "Smart Patient" coaching in Indonesia. Population Council, 2002. http://dx.doi.org/10.31899/rh4.1173.

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Ater, Lynda. The development of a patient satisfaction evaluation system in a family practice setting. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.2116.

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Machiyama, Kazuyo, Joyce Mumah, Caroline Kabiru, et al. Women's perceptions and experiences of family planning by contraceptive methods in Kenya and Bangladesh: Preliminary results. Population Council, 2017. http://dx.doi.org/10.31899/rh4.1073.

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McCabe, Heather. Gender Difference in Working Parents' Perceptions of Work/Family Conflict and the Role of Occupational Prestige. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.2527.

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Gates, Timothy M. Quantitative Analysis of Contributing Factors Affecting Patient Satisfaction in Family Medicine Service Clinics at Brooke Army Medical Center. Defense Technical Information Center, 2008. http://dx.doi.org/10.21236/ada493866.

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DiBenedetti, Dana B., T. Michelle Brown, Carla Romano, Claire Ervin, Sandy Lewis, and Sheri Fehnel. Conducting Patient Interviews Within a Clinical Trial Setting. RTI Press, 2018. http://dx.doi.org/10.3768/rtipress.2018.op.0054.1808.

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Abstract:
Qualitative data centered on patients’ experiences and perspectives typically go uncollected in clinical trial settings. Yet patients’ treatment experiences offer complementary insights and context on topics such as disease management, treatment gaps, and previous treatments outside of those gathered in traditional patient-reported outcome questionnaires. Qualitative interviews can capture patients’ perceptions of treatment needs, more fully explore meaningful changes experienced as a result of treatment, and reveal outcomes that are most important to patients. Asking patients detailed questions can provide insight into the “why” of a patient’s expressed thought or feeling. The inclusion of patient interviews within clinical trials is a relatively new and evolving field of research. This article delineates the types of data that may be collected during interviews with clinical trial participants and outlines two approaches to conducting qualitative research in the clinical trial setting, with a focus on maximizing the value of the resulting data.
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