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Reducing Maximal Support in OCD: Efficacy of Stepped-Care Online CBT

S

Shanghai Mental Health Center

Status

Completed

Conditions

Obsessive Compulsive Disorder (OCD)

Treatments

Other: stepped-care Internet-based cognitive behavioral therapy(SC-ICBT)
Other: Cognitive Behavioral Group Therapy (CBGT)
Drug: conventional medical treatment (TAU)

Study type

Interventional

Funder types

Other

Identifiers

NCT06659094
2024-TX-004

Details and patient eligibility

About

This study is conducted to explore the efficacy and cost-effectiveness of stepped-care internet-based cognitive behavior therapy (sc-ICBT) with reduced support compared to cognitive-behavioral group therapy(CBGT), to identify the optimal transition points for shorter effective stepped treatments, to find clinical indicators that can predict the effectiveness of CBT interventions, and to investigate predictive outcomes.

The main questions the investigators aim to answer are:

  1. Is the reduction in YBOCS scores following stepped-care Internet-based cognitive-behavioral therapy (SC-ICBT) with reduced support non-inferior to that observed in traditional cognitive-behavioral group therapy (CBGT)?
  2. Does SC-ICBT for obsessive-compulsive disorder offer better health economic benefits compared to CBGT?
  3. What is the optimal time point for transitioning to shorter effective stepped care, and what clinical indicators can predict the efficacy of CBT interventions post-treatment?

Full description

SC-ICBT is a therapy combining therapist-guided and semi-self-directed ICBT, with treatment plans adjusted based on patient symptoms. While it aims to be minimally restrictive and low-cost, research shows that low-intensity treatment may miss the mark for patients with severe symptoms or low motivation. High dropout rates and safety concerns are also noted. To address this, the investigators propose starting with high-intensity one-on-one support, reassessing symptoms in the third week, and switching to low-intensity self-guided practice if improvement is seen, otherwise continuing high-intensity support.

In our study, the investigators will conduct a stepped-care Internet-based Cognitive Behavioral Therapy (ICBT) intervention trial with reduced support intensity: Following baseline symptom assessment (Week 0), participants will be allocated to either an online therapy group or an in-person group therapy group. Considering practicality, the study will employ a partially randomized allocation method: for participants who are convenient for both treatment modalities, the investigators will use random numbers to randomly assign them to either the online therapy group or the in-person group therapy group; if participants can only attend one of the treatment groups, the investigators will allocate them based on their preference. The group assignment will be blinded to the assessors. The study will feature two groups for a controlled trial: the experimental group, stepped-care ICBT combined with medication; the control group, cognitive-behavioral group therapy combined with medication. This study is conducted to explore the efficacy and cost-effectiveness of sc-ICBT with reduced support compared to CBGT in China.

The investigators plan to recruit 80 patients and assign them to the SC-ICBT group and the CBGT group for a 6-week intervention, with a follow-up period of 3 months post-intervention. During this period, the investigators will employ questionnaires, scales, functional magnetic resonance imaging (fMRI), and other experimental methods to assess participants' obsessive-compulsive symptoms and treatment outcomes. Concurrently, the investigators will collect data on patients' economic burden and self-reported health status to evaluate the cost effect of SC-ICBT.

Enrollment

95 patients

Sex

All

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Individuals aged between 18 and 50 years, inclusive of both genders;
  2. Presenting primarily with compulsive symptoms that meet the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) criteria for Obsessive-Compulsive Disorder (OCD);
  3. Yale-Brown Obsessive Compulsive Scale (YBOCS) scores ranging from 16 to 31, inclusive;
  4. Have been on a stable regimen of standard anti-compulsive pharmacotherapy for a period of 8 weeks;
  5. Possess a minimum educational level of junior high school;
  6. Demonstrate adequate auditory and visual acuity to perform the assessments required by the study;
  7. The participant and their legal guardian have comprehended the nature of the study and have provided informed consent;
  8. Right-handedness (this criterion applies exclusively to participants undergoing magnetic resonance imaging).

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)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

95 participants in 2 patient groups

stepped-care Internet-based cognitive behavioral therapy(SC-ICBT) combined with medication
Experimental group
Description:
Patients' OCD severity is initially assessed with the Yale-Brown Obsessive Compulsive Scale (YBOCS). After enrollment, patients receive health education, observe symptoms, learn ERP theory, and create exposure lists on a WeChat mini-program for pre-treatment. They perform daily 1-hour ERP exercises for a week, with online status collection by coordinators. After a week, patients receive twice-weekly online ERP guidance from therapists for two weeks. After two and four therapy sessions, YBOCS re-evaluations occur via Tencent Meeting. Based on scores, the next three weeks involve either self-guided ERP or a mix of self-guided and therapist-guided ERP. If patients show over a 25% reduction, therapist guidance is suspended, and they switch to self-guided ICBT for the final three weeks.
Treatment:
Drug: conventional medical treatment (TAU)
Other: stepped-care Internet-based cognitive behavioral therapy(SC-ICBT)
Cognitive Behavioral Group Therapy (CBGT) combined with medication
Active Comparator group
Description:
OCD patients will be provided with therapist-guided offline Cognitive Behavioral Group Therapy while they will continue with the medications they already have. A nationally registered psychotherapist, who has undergone systematic professional training, is in charge of a homogeneous closed group and records the sessions live. The treatment takes place in the group psychotherapy room at the Shanghai Mental Health Center, with a group of 6 people, for 6 weeks, twice a week, each session lasting 2 hours. A senior domestic group cognitive therapist supervises the treatment.
Treatment:
Drug: conventional medical treatment (TAU)
Other: Cognitive Behavioral Group Therapy (CBGT)

Trial contacts and locations

1

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Central trial contact

Yuhan Yang

Data sourced from clinicaltrials.gov

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