Reminiscence Therapy on Depression, Self Esteem, Life Satisfaction, and Loneliness of the Elderly

May 14, 2012 updated by: Li Juan, Chinese Academy of Sciences

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

Status

Unknown

Conditions

Intervention / Treatment

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

Interventional

Enrollment (Anticipated)

60

Phase

  • Phase 2

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Beijing
      • Beijing, Beijing, China, 100101
        • Recruiting
        • Chinese Academy of Sciences, Institute of Psychology, Center on Ageing Psychology, Key Lab of Mental Health
        • Contact:
        • Contact:
        • Principal Investigator:
          • Juan Li, PhD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

60 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

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.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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:
  • life review
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.

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

Secondary Outcome Measures

Outcome Measure
Time Frame
Change in self esteem using the Self-Esteem Scale (SES)
Time Frame: the 6th and 18th week
the 6th and 18th week
Change in life satisfaction using the Life Satisfaction Index A (LSI-A)
Time Frame: the 6th and 18th week
the 6th and 18th week
Change in loneliness using Russell's UCLA Loneliness Scale
Time Frame: the 6th and 18th week
the 6th and 18th week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Juan Li, PhD, Chinese Acad Sci, Inst Psychol, Ctr Ageing Psychol, Key Lab Mental Hlth

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

October 1, 2011

Primary Completion (Anticipated)

September 1, 2012

Study Completion (Anticipated)

September 1, 2012

Study Registration Dates

First Submitted

March 6, 2012

First Submitted That Met QC Criteria

March 12, 2012

First Posted (Estimate)

March 14, 2012

Study Record Updates

Last Update Posted (Estimate)

May 15, 2012

Last Update Submitted That Met QC Criteria

May 14, 2012

Last Verified

May 1, 2012

More Information

Terms related to this study

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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