Effect of SC-ICBT for Adults With OCD：A Three-Arm Randomized Controlled Trial

• Status: Not yet recruiting
• Trial end date: 2024-06-30
• Target enrollment: 0
• Participant gender: All

Summary

This study aims to investigate the efficacy and cost-effectiveness of SC-ICBT related to CBGT and TAU for adults with OCD in China.

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Shanghai Mental Health Center

Criteria

Inclusion Criteria:

1. Age between 18 and 50 years

2. Satisfied with the diagnostic criteria for OCD in DSM-V.

3. 16≤YBOCS score ≤31

4. Taking medication stably for 8 weeks

5. Education level ⩾6 years

6. Has sufficient audiovisual skills to complete the necessary examinations for the study.

7. Right-handed (this criterion is for fMRI subjects only)

8. Subjects and their guardians understood the study and signed informed consent.

Exclusion Criteria:

1. Satisfied with the diagnostic criteria for a mental disorder in DSM-V other than OCD.

2. Obsessive-compulsive symptoms were too severe to participate in the experiment.

3. High risk of suicide.

4. Severe central system or physical disease

5. Pregnant women or women that getting ready for being pregnant and lactating.

6. Other treatments being performed.

7. Uncooperative or unable to complete treatment

8. With metal implants in the body, such as pacemakers, intracranial silver clips, metal dentures, arterial stents, arterial clips, joint metal fixation, or other metal implants, etc. (this criterion is for fMRI subjects only)