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Study on the Efficacy Mechanism of Natural Psychotherapy for Neurosis

Sponsor
Beijing HuiLongGuan Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05552014
Collaborator
(none)
80
Enrollment
1
Location
2
Arms
25
Anticipated Duration (Months)
3.2
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

We explore objective indicators of the efficacy of natural psychotherapy in the treatment of disorders such as obsessive-compulsive disorder

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Natural Psychotherapy
  • Behavioral: Mental Health Education
 N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
80 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Research on the Efficacy Mechanism of Natural Psychotherapy for Neurosis
Actual Study Start Date :
May 1, 2022
Anticipated Primary Completion Date :
Dec 1, 2023
Anticipated Study Completion Date :
Jun 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Natural Psychotherapy

Intervention using natural psychotherapy for OCD patients for two to three hours once a week for eight weeks

Behavioral: Natural Psychotherapy
Natural psychotherapy is based on "Morita therapy" and is a psychotherapy that fully reflects the characteristics of Chinese culture, taking into account the Chinese cultural background and actual clinical characteristics.
Placebo Comparator: Mental Health Education

Mental health education was given to another group of OCD patients for two hours once a week for eight weeks

Behavioral: Mental Health Education
Mental Health Education Seminar

Outcome Measures

Primary Outcome Measures

  1. Clinical symptoms [12 weeks]

    Obsessive-compulsive symptoms were assessed according to the Obsessive-Compulsive Scale

  2. Cognitive function [12 weeks]

    Cognitive function as assessed by RBANS

  3. Prospective memory [12 weeks]

    Whether the patient's prospective memory is effectively improved using EEG and NMR

  4. Mood and behavior [12 weeks]

    Mood changes judged using gait and face recognition

Eligibility Criteria

Criteria

Ages Eligible for Study:
15 Years to 50 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

  • Have a diagnosis of obsessive-compulsive disorder or compulsive behavior

  • Duration of symptoms for not less than 12 months

  • Age 15-50 years old.

  • You can participate in the whole experiment and offline assessment in Beijing

Exclusion Criteria:

  • Documented disease of physical diseases including, but not limited to stroke, tumor, Parkinson's disease, Huntington's disease, seizure, epilepsy, history of brain trauma

  • Subjects who suffered from alcohol or illegal drug abuse/dependence

Contacts and Locations

Locations

Site City State Country Postal Code
1 Institute of Psychology, Chinese Academy of Sciences Beijing China 100096

Sponsors and Collaborators

  • Beijing HuiLongGuan Hospital

Investigators

  • Principal Investigator: Xiang Y Zhang, M.D, Ph.D, Institute of Psychology, Chinese Academy of Science

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Xiang Yang Zhang, Professor, Beijing HuiLongGuan Hospital
ClinicalTrials.gov Identifier:
NCT05552014
Other Study ID Numbers:
  • CASPsy5
First Posted:
Sep 23, 2022
Last Update Posted:
Sep 23, 2022
Last Verified:
Sep 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Xiang Yang Zhang, Professor, Beijing HuiLongGuan Hospital
obsessive-compulsive disorder
natural psychotherapy
Additional relevant MeSH terms:
Compulsive Personality Disorder
Obsessive-Compulsive Disorder

Study Results

No Results Posted as of Sep 23, 2022