Depression Clinical Trial
Official title:
The Effect of Combination Mindfulness Spiritual-Based Cognitive Therapy Plus Hypnosis on Levels of Cortisol, Serotonin, and Depression Degree in HIV Patients With Depression
Verified date | December 2022 |
Source | Health Technology Institute of Cendekia Utama Kudus |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
HIV/AIDS patients are at risk for depression, a multifactorial disorder with signs and symptoms that affect the cognitive, affective, behavioral, and somatic areas. This study used Randomized Controlled Clinical Trials (RCT). Main hypothesis: A combination of spiritual awareness-based cognitive therapy (MSBCT) plus hypnotic interventions can reduce depression degree scores by reducing cortisol levels and increasing serotonin levels in HIV patients with depression. Small hypothesis 1. There was a decrease in cortisol levels after being given the MSBCT plus hypnosis combination intervention in HIV patients with depression; 2. There was an increase in serotonin levels after being given the MSBCT plus hypnosis combination intervention in HIV patients with depression; 3. There was a decrease in depression degree scores after being given the MSBCT plus hypnosis combination intervention in HIV patients with depression; 4. There was a higher reduction in cortisol levels in the intervention group compared to the control group in HIV patients with depression; 5. There was a higher increase in serotonin levels in the intervention group compared to the control group in HIV patients with depression; 6. There was a higher reduction in scores degree of depression in the intervention group compared to the control group in HIV patients with depression; 7. Decreased cortisol levels and increased serotonin levels affect depression degree scores in HIV patients with depression; 8. MSBCT plus hypnosis combination intervention is a factor that can affect depression degree scores reduction in HIV patients with depression;
Status | Completed |
Enrollment | 62 |
Est. completion date | April 10, 2021 |
Est. primary completion date | April 10, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility | Inclusion Criteria: 1. HIV patients with mild-moderate depression; 2. Receiving ARV therapy; 3. Islam; 4. Aged 18-60 years; 5. Not taking steroid and serotonin medications; 6. Willing to sign the informed consent; Exclusion Criteria: 1. Having a history of immune disorders or allergies; 2. Currently undergoing hormonal or corticosteroid therapy; 3. Patients who used herbal medicine 2 weeks before the study; 4. Patients with psychiatric comorbidities and emergency conditions. |
Country | Name | City | State |
---|---|---|---|
Indonesia | Eny Pujiati | Kudus | Middle Java |
Lead Sponsor | Collaborator |
---|---|
Health Technology Institute of Cendekia Utama Kudus |
Indonesia,
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* Note: There are 31 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Decreased serum cortisol levels | Serum cortisol levels were measured using the ELISA kit catalog method number CO103S in the GAKI laboratory, Faculty of Medicine, Diponegoro University - Semarang - Indonesia | Before intervention, and 8 weeks after intervention | |
Primary | Increased serum serotonin levels | Serum serotonin levels were measured using the ELISA kit catalog method number E - EL-H0033 in the GAKI laboratory, Faculty of Medicine, Diponegoro University - Semarang - Indonesia | Before intervention, and 8 weeks after intervention | |
Primary | Decreased degree scores of depression | Depression degree scores were measured using the Beck Depression Inventory (BDI) II | Before intervention, and 8 weeks after intervention |
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