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The Study of Mindfulness Based Cognitive Therapy and Obsessive-Compulsive Disorder

Primary Purpose

Obsessive-Compulsive Disorder

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Mindfulness-based Cognitive Therapy
Psycho-education Program
sertraline, fluvoxamine
Sponsored by
Shanghai Mental Health Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obsessive-Compulsive Disorder focused on measuring Mindfulness-Based Cognitive Therapy

Eligibility Criteria

18 Years - 54 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Participants should suffer from clinically OCD symptoms and have a DSM-IV Axis Ⅰ diagnosis of OCD (M.I.N.I.)
  • 12≤ Y-BOCS score ≤25
  • Male or female, 18 years old to 54 years of age
  • Junior middle school education or above
  • Have not yet accepted psychiatric medication, or had received irregular medication treatment and have been discontinued 8 weeks
  • Have enough visual and acoustic ability to complete the inspection required for the study
  • Each patient and his guardian must understand the nature of this study and sign the informed consent form

Exclusion Criteria:

  • meet DSM-IV Axis Ⅰ diagnostic criteria for other psychiatric disorders
  • persons with severe physical disease or central nervous system disease
  • have a strong negative concept or a high risk of suicide
  • substance abuse, pregnancy or the preparation of recently pregnant women and lactating women
  • severe obsessive compulsive symptoms, so that patients can not complete the required assessment and treatment intervention
  • at the same time to accept MECT or other psychological therapy
  • patients had previously received treatment of mindfulness-based intervention, and no significant effect

Sites / Locations

  • Clinical psychiatrist

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Placebo Comparator

Active Comparator

Arm Label

Mindfulness-based Cognitive Therapy

Psycho-education Program

SSRIs Therapy

Arm Description

MBCT group is a treatment group used mindfulness-based cognitive therapy, and guided by two therapists for 10 sessions. Every collection of about 6-8 patients is a closed structural group. Each session lasts 2.5 hours once a week, and has daily homework assignments.

The program is consists of the information and principle of treatment for OCD, group sharing, supporting and discussion.

This is a control group that can choose to use SSRI drugs which the SFDA approved for the treatment of OCD (Sertraline, Fluvoxamine, initial dose of 50 mg).

Outcomes

Primary Outcome Measures

Yale-Brown Obsessive-Compulsive Scale
Yale-Brown Obsessive-Compulsive Scale is a medical semi-structured questionnaire with a total of 10 items that measure the severity of Obsessive thinking and compulsive behavior on a scale of 0 = None; 1 = Sub-threshold; 2 =Mild; 3 =Moderate; and 4 = Severe. The total score is to be got by adding every score of all the items. And the higher the score is, the more severe OC symptoms are.

Secondary Outcome Measures

Hamilton Anxiety Scale
Hamilton Anxiety Scale is the most common other-rating scale for clinical assessment of anxiety status and suitable for adults with anxiety symptoms. There are 14 items with each symptom rated on a five-point Scale.
Hamilton Depression Scale-24
Hamilton Depression Scale-24 is the most common other-rating scale for clinically assessing the state of depression and suitable for adults with depressive symptoms. There are 24 items rated to each symptom and most of the items used 0 to 4 points.

Full Information

First Posted
May 14, 2017
Last Updated
January 5, 2020
Sponsor
Shanghai Mental Health Center
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1. Study Identification

Unique Protocol Identification Number
NCT03179839
Brief Title
The Study of Mindfulness Based Cognitive Therapy and Obsessive-Compulsive Disorder
Official Title
The Study of Mindfulness Based Cognitive Therapy and Obsessive-Compulsive Disorder
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
January 20, 2017 (Actual)
Primary Completion Date
November 20, 2018 (Actual)
Study Completion Date
July 20, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Shanghai Mental Health Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The primary objective of the study is to evaluate the clinical curative effect of MBCT to reduce obsessive and compulsive symptoms. Moreover, the investigators will also explore a MBCT manual for Chinese patients with OCD, which can be widely applied to the clinical practice. There are two parts of the study. The first part is a qualitative research with two pilot MBCT groups. The second part of this study is a single-blind randomized controlled trial with three study arms: one - third of participants receive group mindfulness-based cognitive therapy led by trained MBCT psychotherapists or psychiatrists in addition to medication, one - third of participants receive group psycho-education program and one - third of participants receive drug therapy as usual. All participants have 10 sessions intervention and assessments.
Detailed Description
The qualitative research will use grounded theory path to interview therapists and patients for 60 minutes in the baseline, after 5 weeks treatments and after the 10 weeks treatments. The subjective experience of the therapists and patients in two pilot MBCT groups will be described and explained. And the entire process of treatments will be participatory observed. In the second part of the study, all patients will take blood test and functional magnetic resonance imaging (fMRI) scan in the baseline and after 10 weeks, to gather data in genetics and imaging features, which can help the study to discover biological indicators of the curative effect. And after the patients and their custodians signed the consent form, all of participants will be blindly assigned to three groups by a predetermined random table which is generated by Microsoft Excel 2010 for ensuring randomly fair distribution across conditions. The investigators will not decode these numbers until the intervention group is assigned. As the research tools, a range of self-rating scales, other-rating scales and behavioral and physiological measures will be mainly applied to assess clinical symptoms of participants at baseline (week 0), mid-treatment (week 4), at the end of acute treatment (week 10), and during the maintenance phase (week 14, 22 and 34). After 10 sessions, all the participants including the non-responders and the responders (ie, decrease in Yale-Brown Obsessive Compulsive Scale [YBOCS] scores ≥ 25%) will enter the maintenance phase for 6 months. The participants in MBCT group will continue MBCT treatments at home. The participants in drug therapy group will continue on their treatment program without changing the type and dosage of medication they have been using. By comparing clinical symptoms, such as obsessive and compulsive symptoms, anxiety, depression, quality of life and other clinical symptoms and behavior, the study will describe the short-term and long-term effects of MBCT in patients with DSM-IV obsessive-compulsive disorder (OCD).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obsessive-Compulsive Disorder
Keywords
Mindfulness-Based Cognitive Therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
123 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Mindfulness-based Cognitive Therapy
Arm Type
Experimental
Arm Description
MBCT group is a treatment group used mindfulness-based cognitive therapy, and guided by two therapists for 10 sessions. Every collection of about 6-8 patients is a closed structural group. Each session lasts 2.5 hours once a week, and has daily homework assignments.
Arm Title
Psycho-education Program
Arm Type
Placebo Comparator
Arm Description
The program is consists of the information and principle of treatment for OCD, group sharing, supporting and discussion.
Arm Title
SSRIs Therapy
Arm Type
Active Comparator
Arm Description
This is a control group that can choose to use SSRI drugs which the SFDA approved for the treatment of OCD (Sertraline, Fluvoxamine, initial dose of 50 mg).
Intervention Type
Behavioral
Intervention Name(s)
Mindfulness-based Cognitive Therapy
Intervention Description
The intervention will be carried out according to the handbook of the Dr. Didonna. There is a Session Agenda from Dr. Didonna for the use of the Instructor and session handouts for the participants. Some records of mindfulness practices will be given to participants for facilitating practice between sessions. Before each session, the instructor needs to review the session agenda and prepare copies of handouts for participants. MBCT instructors were experienced psychotherapists and psychiatrists with several years' expertise in OCD treatment. They had been trained by one of the founders of MBCT, Mark Williams and the founder of MBCT for OCD, Fabrizio Didonna. Supervision will be provided by Dr.Didonna.
Intervention Type
Behavioral
Intervention Name(s)
Psycho-education Program
Intervention Description
As a widely used placebo control condition, the Psycho-Education Program can play an active role through the psychological suggestion and forward thinking mostly. It is designed to be similar with MBCT in level of structure, setting and other non-specific effects of psychological intervention. All instructors will be qualified graduate students who major in clinical psychology with training in cognitive behavioral therapy and psychodynamic therapy.
Intervention Type
Drug
Intervention Name(s)
sertraline, fluvoxamine
Intervention Description
The participants can be adjustable once a week dose and the maximum dose does not exceed the maximum amount of instructions. And benzodiazepine drugs also can be used by the OCD patients with sleep disorders, but not be used continuously for more than two weeks. Besides this, other psychotropic drugs are not allowed to use. The use of drugs in this study are commonly used drugs with good safety, and its common adverse reactions include dry mouth, constipation, nausea, indigestion, dizziness, fatigue, sweating and so on.
Primary Outcome Measure Information:
Title
Yale-Brown Obsessive-Compulsive Scale
Description
Yale-Brown Obsessive-Compulsive Scale is a medical semi-structured questionnaire with a total of 10 items that measure the severity of Obsessive thinking and compulsive behavior on a scale of 0 = None; 1 = Sub-threshold; 2 =Mild; 3 =Moderate; and 4 = Severe. The total score is to be got by adding every score of all the items. And the higher the score is, the more severe OC symptoms are.
Time Frame
Change from baseline up to week 34
Secondary Outcome Measure Information:
Title
Hamilton Anxiety Scale
Description
Hamilton Anxiety Scale is the most common other-rating scale for clinical assessment of anxiety status and suitable for adults with anxiety symptoms. There are 14 items with each symptom rated on a five-point Scale.
Time Frame
Change from baseline up to week 34
Title
Hamilton Depression Scale-24
Description
Hamilton Depression Scale-24 is the most common other-rating scale for clinically assessing the state of depression and suitable for adults with depressive symptoms. There are 24 items rated to each symptom and most of the items used 0 to 4 points.
Time Frame
Change from baseline up to week 34

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
54 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Participants should suffer from clinically OCD symptoms and have a DSM-IV Axis Ⅰ diagnosis of OCD (M.I.N.I.) 12≤ Y-BOCS score ≤25 Male or female, 18 years old to 54 years of age Junior middle school education or above Have not yet accepted psychiatric medication, or had received irregular medication treatment and have been discontinued 8 weeks Have enough visual and acoustic ability to complete the inspection required for the study Each patient and his guardian must understand the nature of this study and sign the informed consent form Exclusion Criteria: meet DSM-IV Axis Ⅰ diagnostic criteria for other psychiatric disorders persons with severe physical disease or central nervous system disease have a strong negative concept or a high risk of suicide substance abuse, pregnancy or the preparation of recently pregnant women and lactating women severe obsessive compulsive symptoms, so that patients can not complete the required assessment and treatment intervention at the same time to accept MECT or other psychological therapy patients had previously received treatment of mindfulness-based intervention, and no significant effect
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yifeng Shen, Senior
Organizational Affiliation
Shanghai Mental Health Center
Official's Role
Study Director
Facility Information:
Facility Name
Clinical psychiatrist
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200030
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No

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The Study of Mindfulness Based Cognitive Therapy and Obsessive-Compulsive Disorder

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