- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01553669
Reminiscence Therapy on Depression, Self Esteem, Life Satisfaction, and Loneliness of the Elderly
The Effects of Reminiscence Therapy on Depression, Self Esteem, Life Satisfaction, and Loneliness of the Elderly in China
The primary hypothesis is, comparing with the control group, reminiscence therapy is significantly and clinically effective to improve the experiment group's depressive symptoms after six weeks therapy, and the efficacy can be maintained on the three months follow-up.
The secondary hypothesis is, comparing with the control group, reminiscence therapy significantly reduce the loneliness and increase the self-esteem and life satisfaction of the experiment group.
Study Overview
Detailed Description
The subjects who are arranged to the experiment group will be intervened using the reminiscence therapy manual proposed by Watt and Cappeliez (2000). According to the manual, the group consisted of six weekly sessions of 90 min each. During each weekly session, the memories recalled focused on a different theme.
Data collection will occur on screening (as for baseline or pre-test), after intervention immediately (as for post-test), and three months after the intervention (as for follow-up). And outcome measures use standardized instruments with demonstrated validity and reliability:
Geriatric Depression Scale (GDS) Rosenberg self-esteem scale (SES) Life Satisfaction Index A (LSI-A) Russell's UCLA Loneliness Scale
Study Type
Enrollment (Anticipated)
Phase
- Phase 2
Contacts and Locations
Study Locations
-
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Beijing
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Beijing, Beijing, China, 100101
- Recruiting
- Chinese Academy of Sciences, Institute of Psychology, Center on Ageing Psychology, Key Lab of Mental Health
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Contact:
- Tingji Chen, master
- Phone Number: (086)18610249921
- Email: Chentj@psych.ac.cn
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Contact:
- Juan Li, PhD
- Phone Number: (086)010-64861622
- Email: lijuan@psych.ac.cn
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Principal Investigator:
- Juan Li, PhD
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- 60 years of age and older;
- A score above 10 and lower than 26 on the Geriatric Depression Scale (GDS);
- A score of 24 or higher on the Mini-Mental State Examination (MMSE);
- Not taking anti-depressant medication or taking part in other psychotherapy when enrolling, if taking anti-depressant medication, must be stabilized on that medication for at least three months;
- Having no problem with communication (such as, can speak fluent mandarin, or if he/she speaks a dialect, his/her dialect can be understood by most of people).
Exclusion Criteria:
- Suicide attempt;
- A diagnosis of cognitive impairment by DSM-Ⅳ, or mental disorders other than depression;
- Alcohol or drug abuse;
- Cannot grantee attending the therapy at a weekly base due to physical impairment, lack of time or unwilling etc.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: reminiscence therapy
Reminiscence therapy is a method of using the memory to protect mental health and improve the quality of life.
|
The subjects who are arranged to the experiment group will be intervened using the reminiscence therapy manual proposed by Watt and Cappeliez (2000).
According to the manual, the group consisted of six weekly sessions of 90 min each.
There will be about four people in each subgroup.
During each weekly session, the memories recalled focused on a different theme.
Other Names:
|
No Intervention: Control group
The participants assigned to the waiting-list as the control group will be treated as before.
After the intervention period, we will conduct reminiscence therapy on them if they ask for.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Change in depression using the Geriatric Depression Scale(GDS)
Time Frame: the 6th and 18th week
|
the 6th and 18th week
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Change in self esteem using the Self-Esteem Scale (SES)
Time Frame: the 6th and 18th week
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the 6th and 18th week
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Change in life satisfaction using the Life Satisfaction Index A (LSI-A)
Time Frame: the 6th and 18th week
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the 6th and 18th week
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Change in loneliness using Russell's UCLA Loneliness Scale
Time Frame: the 6th and 18th week
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the 6th and 18th week
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Juan Li, PhD, Chinese Acad Sci, Inst Psychol, Ctr Ageing Psychol, Key Lab Mental Hlth
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2009BAI77B03
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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