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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

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01553669
Enrollment
60
Registered
2012-03-14
Start date
2011-10-31
Completion date
2012-09-30
Last updated
2012-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression

Brief summary

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.

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

Interventions

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.

Sponsors

Chinese Academy of Sciences
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. 60 years of age and older; 2. A score above 10 and lower than 26 on the Geriatric Depression Scale (GDS); 3. A score of 24 or higher on the Mini-Mental State Examination (MMSE); 4. 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; 5. 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

1. Suicide attempt; 2. A diagnosis of cognitive impairment by DSM-Ⅳ, or mental disorders other than depression; 3. Alcohol or drug abuse; 4. Cannot grantee attending the therapy at a weekly base due to physical impairment, lack of time or unwilling etc.

Design outcomes

Primary

MeasureTime frame
Change in depression using the Geriatric Depression Scale(GDS)the 6th and 18th week

Secondary

MeasureTime frame
Change in self esteem using the Self-Esteem Scale (SES)the 6th and 18th week
Change in life satisfaction using the Life Satisfaction Index A (LSI-A)the 6th and 18th week
Change in loneliness using Russell's UCLA Loneliness Scalethe 6th and 18th week

Countries

China

Contacts

Primary ContactTingji Chen, master
Chentj@psych.ac.cn(086)18610249921

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 25, 2026