- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06301269
A Study on Self-Compassion,Depression,and Quality of Life Among Primary Caregivers of People With Dementia
The goal of this observational study is to investigate the correlation between self-compassion, depression, and quality of life among primary caregivers of persons with dementia.
The main questions it aims to answer are:
- What is the current status of self-compassion, depression, and quality of life among primary caregivers of persons with dementia?
- Are there differences in self-compassion, depression, and quality of life among primary caregivers of persons with dementia based on different background variables?
- What is the correlation between self-compassion, depression, and quality of life among primary caregivers of persons with dementia?
Participants will fill out the questionnaire to complete the study.
Study Overview
Detailed Description
The study design of this research is cross-sectional. The participants are primary caregivers of dementia patients diagnosed by specialists, aged 18 and above, who spend 8 hours or more daily (including overnight caregivers) providing care. Data is collected using instruments including the Self-Compassion Scale, the PHQ-9 Scale (Patient Health Questionnaire,PHQ-9), and the Quality-of-Life Scale to investigate the relationship between self-compassion, depression, and quality of life among primary caregivers of dementia patients.
The study uses independent samples t-tests and one-way ANOVA( analysis of variance,ANOVA) to explore differences in self-compassion, depression, and quality of life among primary caregivers of dementia patients based on different background variables. Pearson correlation is used to analyze the relationships between these variables. Finally, linear regression is used to predict the performance of primary caregivers of dementia patients in self-compassion, depression, and quality of life.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Wen Lin Ye
- Phone Number: 262788 02-2312 3456
- Email: vovo951357@ntuh.gov.tw
Study Locations
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Taipei, Taiwan, 100
- Recruiting
- National Taiwan University Hospital
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Contact:
- wen lin YE
- Phone Number: +886-2312-3456
- Email: vovo951357@ntuh.gov.tw
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- primary caregivers of dementia patients diagnosed by specialists
- aged 18 and above
- who spend 8 hours or more daily (including overnight caregivers) providing care
Exclusion Criteria:
- Those who do not agree to participate in the research
- Caregivers in a paid relationship with dementia patients, such as foreign domestic helpers and government-provided resident care attendant
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self-Compassion Scale
Time Frame: The participants will spend 5-10 minutes completing the questionnaire during the study
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The self-compassion score, measured using the Self-Compassion Scale, reflects the level of self-compassion among primary caregivers of people with dementia.
|
The participants will spend 5-10 minutes completing the questionnaire during the study
|
|
PHQ-9 Scale
Time Frame: The participants will spend 5-10 minutes completing the questionnaire during the study
|
The PHQ-9 Scale, measured using the PHQ-9 Scale, reflects the level of depression among primary caregivers of people with dementia.
|
The participants will spend 5-10 minutes completing the questionnaire during the study
|
|
Quality-of-Life Scale
Time Frame: The participants will spend 5-10 minutes completing the questionnaire during the study
|
The Quality-of-Life Scale , measured using the Quality-of-Life Scale , reflects the level of Quality-of-Life among primary caregivers of people with dementia.
|
The participants will spend 5-10 minutes completing the questionnaire during the study
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 202312124RINA
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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