Depression, Anxiety Clinical Trial
Official title:
Morita Therapy Combined With Xingnao Kaiqiao Acupressure for Relieving Depressive Symptoms During COVID-19: A Randomized Controlled Study
NCT number | NCT05631145 |
Other study ID # | MTXKSA |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | May 3, 2020 |
Est. completion date | October 15, 2020 |
Verified date | November 2022 |
Source | Central South University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Social isolation related mental health problems have raised many concerns during the COVID-19 outbreaks. Mental health care for people in quarantined hotels is in urgent need, but concrete program is rarely reported. Morita therapy and acupressure have been identified as effective treatments for regulating mood and sleep. The study aimed to examine whether Morita therapy (MT) combined with Xingnao Kaiqiao self-administered acupressure (XKSA) could improve depressive, anxiety symptoms and sleep quality in isolated people with depressive symptoms.
Status | Completed |
Enrollment | 59 |
Est. completion date | October 15, 2020 |
Est. primary completion date | October 1, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: 1. age 18 to 65 years; 2. a PHQ-9 score of > 4 (indicative of mild depression); 3. shinkeishitsu-type neurosis including introspective, sensitive, serious, careful, timid, cautious, perfectionistic, or rigid character, assessed by the Diagnostic Interview of Morita shinkeishitsu (DIM); 4. absence of any problems involving injuries, inflammation, or space-occupying lesions at the locations of the acupoints; 5. ability to understand the trial process; 6. no engagement in other forms of activities to improve mood and sleep (e.g., Tai Chi, yoga, and mindfulness meditation) in the last three months before and during the trial. Exclusion Criteria: 1. severe physical and psychiatric diseases; 2. inability to complete the trial or use necessary psychiatric medicine; 3. cognitive dysfunction caused by neurodegenerative and neurodevelopmental disorders, such as dementia, mental retardation, and autism spectrum disorder; 4. self-injurious or suicidal risk; 5. positive COVID-19 nucleic acid test results. |
Country | Name | City | State |
---|---|---|---|
China | Shenzhen Hospital of Integrated Traditional Chinese and Western Medicine | Shenzhen |
Lead Sponsor | Collaborator |
---|---|
Renrong Wu |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in the Patient Health Questionnaire 9-item depression scale (PHQ-9) | The PHQ-9 is a self-report scale which scored each of the DSM-IV diagnostic criteria for major depressive disorders (MDD) from 0 (not at all) to 3 (nearly every day) and total scores of 5, 10, 15, 20 represent mild, moderate, moderately severe, and severe depression, respectively. | Before and after 2-week treatment immediately. | |
Primary | Changes in the Generalized Anxiety Disorder 7-item (GAD-7) | The GAD-7, comprising seven items scored from 0 to 3 each, is a self-rating scale for generalized anxiety disorder. A total score of 5, 10, or 15 indicated mild, moderate, or severe anxiety symptoms, respectively | Before and after 2-week treatment immediately. | |
Primary | Changes in the Insomnia Severity Index (ISI) | The ISI could evaluate the severity of current insomnia problems with 7 self-rating items involving staying asleep, falling asleep, waking early morning, noticeability of these problems, distress and daily functioning interference caused by these problems, and sleep satisfaction. A total score ranged from 0 to 28 and cutoff points of 8, 15, and 22 representing subthreshold, moderate, and severe insomnia, respectively | Before and after 2-week treatment immediately. |
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