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Recruiting NCT07701616

NCT07701616 Digital Mindfulness-Based Therapy for Obsessive-Compulsive Disorder

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Clinical Trial Summary
NCT ID NCT07701616
Status Recruiting
Phase
Sponsor Central South University
Condition Obsessive-Compulsive Disorder
Study Type INTERVENTIONAL
Enrollment 150 participants
Start Date 2026-07-15
Primary Completion 2027-09-01

Eligibility & Interventions

Sex All sexes
Min Age 12 Years
Max Age 65 Years
Study Type INTERVENTIONAL
Interventions
Digital Mindfulness-Based TherapyRoutine Pharmacological Treatment

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 150 participants in total. It began in 2026-07-15 with a primary completion date of 2027-09-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This randomized controlled trial aims to evaluate the effects of digital mindfulness-based therapy in people with obsessive-compulsive disorder and to explore its possible psychological and neurophysiological mechanisms. A total of 150 participants with a primary diagnosis of obsessive-compulsive disorder will be randomly assigned in a 1:1:1 ratio to one of three groups: digital mindfulness-based therapy, routine pharmacological treatment, or digital mindfulness-based therapy combined with routine pharmacological treatment. The digital mindfulness-based therapy program will last for 6 weeks and will be delivered through a mobile mini-program using structured video and audio lessons, guided mindfulness practices, supervised weekly learning, and home practice. Participants in the pharmacological treatment group will receive routine pharmacological treatment for obsessive-compulsive disorder, and participants in the combined group will receive both interventions. Changes in obsessive-compulsive symptoms, mindfulness, emotional symptoms, and other psychological outcomes will be assessed during treatment and follow-up. Heart rate variability will be assessed at baseline and weekly during the 6-week intervention. Electroencephalography will be assessed at baseline, at the end of the 6-week intervention, and at the 3-month and 6-month follow-up assessments to explore neurophysiological changes associated with treatment.

Eligibility Criteria

Inclusion Criteria: 1. A primary diagnosis of obsessive-compulsive disorder according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5). 2. Aged 12 to 65 years. 3. Primary school education or above and able to understand the study procedures and complete the required assessments. 4. Willing and able to provide written informed consent. For participants under 18 years of age, written informed consent will also be obtained from a parent or legal guardian. 5. Participants who are already receiving psychotropic medication must have maintained a stable medication regimen for at least 4 weeks before enrollment. Any clinically necessary medication changes during the study will be documented. Exclusion Criteria: 1. Current or lifetime diagnosis of schizophrenia spectrum disorder, bipolar disorder, substance use disorder, or personality disorder. 2. Severe physical illness or central nervous system disease that may interfere with participation in the study. 3. Severe suicidal ideation or suicidal behavior within the past month. 4. Pregnancy, planned pregnancy, or breastfeeding. 5. Concurrent participation in another psychotherapy program or clinical trial. 6. Mindfulness practice within the past month. 7. Inability to understand or comply with the study procedures.

Contact & Investigator

Central Contact

Chen Pan, Dr

✉ 758933968@qq.com

📞 86-0731-88618487

Frequently Asked Questions

Who can join the NCT07701616 clinical trial?

This trial is open to participants of all sexes, aged 12 Years or older, up to 65 Years, studying Obsessive-Compulsive Disorder. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07701616 currently recruiting?

Yes, NCT07701616 is actively recruiting participants. Contact the research team at 758933968@qq.com for enrollment information.

Where is the NCT07701616 trial being conducted?

This trial is being conducted at Changsha, China, Changsha, China.

Who is sponsoring the NCT07701616 clinical trial?

NCT07701616 is sponsored by Central South University. The trial plans to enroll 150 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology