| Condition or disease | Intervention/treatment |
|---|---|
| Demoralization | Other: No intervention will be provided as this study is a cross-sectional observational study. |
Show detailed description
| Study Type : | Observational |
| Estimated Enrollment : | 200 participants |
| Observational Model: | Case-Only |
| Time Perspective: | Cross-Sectional |
| Official Title: | Demoralization Among Palliative Care Patients and Their Family Caregivers in Hong Kong: A Pilot Study |
| Actual Study Start Date : | November 26, 2018 |
| Estimated Primary Completion Date : | September 25, 2019 |
| Estimated Study Completion Date : | November 26, 2019 |
| Group/Cohort | Intervention/treatment |
|---|---|
|
Palliative care patients and their family caregivers
The present study is a cross-sectional study with single group study design. Only palliative care patients and their family caregivers will be recruited.
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Other: No intervention will be provided as this study is a cross-sectional observational study.
This item is not applicable because this study is a cross-sectional observational study and no intervention will be provided to participants.
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| Ages Eligible for Study: | Child, Adult, Older Adult |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
For palliative care patients
Inclusion Criteria:
Exclusion Criteria:
-Patients who are assessed by social workers as emotionally too distressful for participating in the research.
For caregivers
Inclusion criteria:
-Caregivers must be the primary family caregivers of the patients
Exclusion criteria:
-Caregivers who are assessed by social workers as emotionally too distressful for participating in the research.
| Contact: Chi Ho Wallace Chan, BSoc, Ph.D | (852) 3943-1518 | chchan@swk.cuhk.edu.hk |
| Hong Kong | |
| Bradbury Hospice (BBH) | Recruiting |
| Hong Kong, Hong Kong, no postal address available in | |
| Contact: Kit ming Jamie Wan (852) 2636-7270 wkm084@ha.org.hk | |
| Principal Investigator: | Chi Ho Wallace Chan, BSoc, Ph.D | Chinese University of Hong Kong |
| Tracking Information | |||||
|---|---|---|---|---|---|
| First Submitted Date | March 25, 2019 | ||||
| First Posted Date | July 5, 2019 | ||||
| Last Update Posted Date | July 5, 2019 | ||||
| Actual Study Start Date | November 26, 2018 | ||||
| Estimated Primary Completion Date | September 25, 2019 (Final data collection date for primary outcome measure) | ||||
| Current Primary Outcome Measures |
Demoralization of patients and caregivers [ Time Frame: This is a one-time self-reported assessment which will take less than 15 minutes to complete. ] Demoralization of patients and caregivers will be measured by the Chinese version of Demoralization Scale (DS).The instrument comprises of 24 items and each item is rated on a 4-point Likert-type scale that ranged from 1 (very disagreed) to 5 (very agreed). Items for each responses will be summed up to create a total score ranging from 0 to 30. The DS also provides 5 subscores, namely, loss of meaning and purpose, dysphoria, disheartenment, helplessness and sense of failure. A higher total score indicates a higher level of demoralization
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| Original Primary Outcome Measures | Same as current | ||||
| Change History | No Changes Posted | ||||
| Current Secondary Outcome Measures |
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| Original Secondary Outcome Measures | Same as current | ||||
| Current Other Pre-specified Outcome Measures | Not Provided | ||||
| Original Other Pre-specified Outcome Measures | Not Provided | ||||
| Descriptive Information | |||||
| Brief Title | Demoralization Among Palliative Care Patients and Their Family Caregivers in Hong Kong: A Pilot Study | ||||
| Official Title | Demoralization Among Palliative Care Patients and Their Family Caregivers in Hong Kong: A Pilot Study | ||||
| Brief Summary | This study aims to explore the prevalence of demoralization among palliative care patients and family caregivers in Hong Kong and examines psychosocial factors associated with demoralization. We hypothesized that higher depression, caregiving strain and caregiver support needs would lead to higher demoralization, and greater perceived family support was associated with lower demoralization among patients and family caregivers. | ||||
| Detailed Description |
Literature Review: Demoralization in palliative care Palliative care patients (PCP) and their family caregivers are always confronted with death and dying issues. The nature of terminal illness may lead to their experience of demoralization. The importance of addressing the demoralization syndrome among PCP was first proposed by Clarke and Kissane (2002). A systematic review reported that the prevalence of demoralization is about 13% to 18% among palliative care patients (Robinson, Kissane, Brooker & Burney, 2016). Only one study examined the prevalence of demoralization among family caregivers of PCP and that aro10% of them suffered from moderate to severe demoralization (Hudson, Thomas, Trauer, Remedios, & Clarke, 2011). PCP and family caregivers may find it difficult to cope with the challenges associated with the terminal illness, and that they may experience a form of existential distress, which is characterized by a sense of meaninglessness, hopelessness and helplessness (Figueriredo, 2013; Robinson, et al., 2016). Demoralization was considered as a key cause of developing suicidal ideations (Julião, Nunes & Barbosa, 2016). Conceptualization and definition of demoralization Kissane (2000) conceptualized demoralization as a syndrome with the following diagnostic criteria: 1. The experience of emotional distress such as hopelessness and having meaning and purpose in life lost; 2. Attitudes of helplessness, failure, pessimism, and lack of a worthwhile future; 3. Reduced coping to respond differently; 4. Social isolation and deficiencies in social support; 5.Persistence if the above-mentioned phenomena across 2 or more weeks; and 6. Features of major depression have not superseded as the primary disorder (Robinson et al., 2016, p.96). Demoralization should be differentiated from depression, e.g. demoralized patients may still enjoy the present moment but feel despair towards future (Clarke & Kissane, 2002; Kissane & Doolittle, 2015). Demoralization may exist independently but can also co-exist with depression. Previous studies showed that 14-27.4% of patients were demoralized but not depressive, while 21.7-33% patients experienced both demoralization and depression (Fang et al., 2014). Factors associated with demoralization Previous studies showed that demoralization was associated with various socio-economic, physical and psychosocial factors. High demoralization was associated with reduced quality of life, emotional and existential distress (e.g. depression, anxiety and desire for hastened death, hopelessness, helplessness and loss of meaning) and declining physiological functions (e.g. pain, fatigue and sleep disorders) (Robinson, Kissane, Brooker & Burney, 2015; Tang, Wang & Chou, 2015). A strong relationship was also found between demoralization and social functioning (Kissane and Doolittle, 2015; Robinson et al., 2015; Tang et. al, 2015). Furthermore, demoralization was found associated with sociodemographic, spiritual and familial factors, such as unemployment, sex, family dysfunction, spiritual problem and dimensions to a person's life (Lee et al., 2011; Li et al, 2017; Kissane and Doolittle, 2015; Robinson et al., 2015). Demoralization has been studied in the western societies in the past decade but little has been known about demoralization prevalence among palliative care patients and family caregivers in Hong Kong. As demoralization is a newly introduced concept, there is limited understanding on its epidemiology and how it can be minimized among PC patients and caregivers. It is thus important to conduct a pilot study in Hong Kong to explore the prevalence of demoralization and factors associated with demoralization. Objectives:
Methods: This study targets to recruit 200 palliative care patients (PCP) and family caregivers who are newly referred to the Medical Social work department of Bradbury Hospice. This study will employ a mixed method design to achieve the study objectives. For quantitative arm, patients and caregivers will be asked to complete a survey respectively, which include different validated instruments. Assistance will be given for completing the survey if necessary. For patient questionnaire, we will include the Chinese version of Demoralization Scale (Hung et al., 2010), the 10-item version of Center for Epidemiological Studies Depression (CES-D), and the Family subscale of the Chinese version of Multidimensional Scale of Perceived Social Support. For the caregiver's questionnaire, similar to the patient questionnaire, we plan to include the Demoralization Scale and CES-D, but we also include the Chinese version of Modified Caregivers' Strain Index and the Carer Support Needs Assessment tool (CSNAT). A total of 200 patients and caregivers will be recruited. Data will be entered into SPSS for analysis. For qualitative arm, individual interviews will be conducted with PCP and caregivers by a trained research assistant. 6 PCP and 6 family caregivers will be purposively selected for interview based on their demoralization level which was reflected from their demoralization scores in the quantitative data. (i.e. 3 patients and 3 family caregivers from each of the following groups: Low demoralization and high demoralization group). Data Management and analysis: All data will be stored confidentially in order to protect participant's privacy. Quantitative data will be entered to SPSS for data analysis. Descriptive, bivariate correlations bivariate correlations and regression analysis will be conducted and missing data will be handled by mean substitution. For interviews data, all the audio-recorded interviews will be transcribed to text for data analysis. Thematic analysis will be conducted to identify the key themes. |
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| Study Type | Observational | ||||
| Study Design | Observational Model: Case-Only Time Perspective: Cross-Sectional |
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| Target Follow-Up Duration | Not Provided | ||||
| Biospecimen | Not Provided | ||||
| Sampling Method | Non-Probability Sample | ||||
| Study Population | This study targets palliative care patients of Bradbury Hospice (BBH) and their family caregivers who are newly referred to the Medical Social Work Department of Bradbury Hospice. | ||||
| Condition | Demoralization | ||||
| Intervention | Other: No intervention will be provided as this study is a cross-sectional observational study.
This item is not applicable because this study is a cross-sectional observational study and no intervention will be provided to participants.
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| Study Groups/Cohorts | Palliative care patients and their family caregivers
The present study is a cross-sectional study with single group study design. Only palliative care patients and their family caregivers will be recruited.
Intervention: Other: No intervention will be provided as this study is a cross-sectional observational study.
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| Publications * |
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |||||
| Recruitment Status | Recruiting | ||||
| Estimated Enrollment |
200 | ||||
| Original Estimated Enrollment | Same as current | ||||
| Estimated Study Completion Date | November 26, 2019 | ||||
| Estimated Primary Completion Date | September 25, 2019 (Final data collection date for primary outcome measure) | ||||
| Eligibility Criteria |
For palliative care patients Inclusion Criteria:
Exclusion Criteria: -Patients who are assessed by social workers as emotionally too distressful for participating in the research. For caregivers Inclusion criteria: -Caregivers must be the primary family caregivers of the patients Exclusion criteria: -Caregivers who are assessed by social workers as emotionally too distressful for participating in the research. |
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| Sex/Gender |
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| Ages | Child, Adult, Older Adult | ||||
| Accepts Healthy Volunteers | Yes | ||||
| Contacts |
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| Listed Location Countries | Hong Kong | ||||
| Removed Location Countries | |||||
| Administrative Information | |||||
| NCT Number | NCT04006327 | ||||
| Other Study ID Numbers | 2018.448 | ||||
| Has Data Monitoring Committee | No | ||||
| U.S. FDA-regulated Product |
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| IPD Sharing Statement |
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| Responsible Party | Wallace Chi Ho Chan, Chinese University of Hong Kong | ||||
| Study Sponsor | Chinese University of Hong Kong | ||||
| Collaborators | Bradbury Hospice | ||||
| Investigators |
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| PRS Account | Chinese University of Hong Kong | ||||
| Verification Date | July 2019 | ||||