Mental Health Clinical Trial
Official title:
The Impact of Group-based Positive Psychotherapy in Psychological Resilience of Only-child-lost People: A Randomized Controlled Trial
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 |
Verified date | January 2023 |
Source | Central South University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
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. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Central South University |
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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