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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05703529
Other study ID # 2015058
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2016
Est. completion date October 31, 2016

Study information

Verified date January 2023
Source Central South University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A randomized controlled trial was conducted to evaluate the effectiveness of group-based positive psychotherapy on psychological resilience, depression, well-being, sleep quality, dehydroepiandrosterone in only-child-lost people. A total of 80 only-child-lost people who met the inclusion and exclusion criteria were expected to recruit. There were six weeks in the intervention, including positive introduction, positive reaction, gratitude, meaningful, three good things, and using personal strength. The measurements were conducted at the baseline, immediately after the intervention, 3-month after the intervention.


Recruitment information / eligibility

Status Completed
Enrollment 68
Est. completion date October 31, 2016
Est. primary completion date October 31, 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 49 Years and older
Eligibility Inclusion Criteria: 1. having only one child or legally adopting; 2. No surviving children; 3. basic language expression and comprehension skills; 4. the score of Connor-Davidson Resilience Scale is lower than 82 Exclusion Criteria: 1. in the acute bereavement period (<6 months); 2. unable to participate in activities due to severe physical illness; 3. having diagnosis of sever mental illness; 4. receiving other psychological therapy.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Positive Psychotherapy
A 6-week group-based positive psychotherapy was conducted in this group. The themes of each week include positive introduction, three good things and positive reactions, gratitude, positive memory, identifying personal strengths and utilizing strengths.
Other:
Usual Care
Usual Care means treating as usual, including a regular home visit.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Central South University

Outcome

Type Measure Description Time frame Safety issue
Primary Change of psychological resilience It is assessed by Connor-Davidson Resilience Scale. A higher score suggests a higher level of psychological resilience. The range is 0-100. Baseline, immediately after the intervention, 3-month after the intervention
Secondary Change of depressive symptoms It is measured by Zung Self-rating Depression Scale with a higher score suggesting a more severe of depressive symptoms Baseline, immediately after the intervention, 3-month after the intervention
Secondary Change of index of well-being It is measured by Campbell's Index of Well-being. A high score indicates a high level of well-being. Baseline, immediately after the intervention, 3-month after the intervention
Secondary Change of Dehydroepiandrosterone (DHEA) in saliva Saliva is collected using a saliva collector and assayed using the Elisa assay. After the specimens were collected, they were tested with the Elisa kit of SalimetricsĀ® according to its instructions. Baseline, immediately after the intervention, 3-month after the intervention
Secondary Change of Sleep Quality It is measured by Pittsburgh Sleep Quality Index. If the total score is over 7, the sleep quality is normal, and if the score is over 7, it suggests a low sleep quality Baseline, immediately after the intervention, 3-month after the intervention
Secondary Change of Social Avoidance and Social Distress It is measured by Social Avoidance and Distress Scale. A high score indicates a high level of social avoidance and social distress. Baseline, immediately after the intervention, 3-month after the intervention
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