Art Therapy in an Intensive OCD Program

Sponsor
Sunnybrook Health Sciences Centre (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05855902
Collaborator
(none)
100
1
36.2
2.8

Study Details

Study Description

Brief Summary

The Thompson Centre Intensive Treatment program for individuals with severe Obsessive-Compulsive Disorder was launched in 2017.

The program is focused on the principles and use of Exposure and Response Prevention Therapy (ERP) and Cognitive Behavioural Therapy (CBT) in its work with clients, however it also integrates other treatment approaches in its structure, including Dialectical Behavior Therapy, Mindfulness, Acceptance and Commitment Therapy, and Art Therapy. Clients are expected to participate in Art Therapy group in the same way they are expected to participate in all other groups in the program schedule.

Though clients comment informally on the benefits of Art Therapy as experienced in the program, study is needed to better understand and appreciate the role Art Therapy can play in helping clients with OCD to manage and where possible, ameliorate, the burden of their symptoms.

Although Art Therapy has been researched to some degree, in particular its role in alleviating distress associated with various health and mental health conditions, to date there has been no systematic investigation addressing or supporting patients'/clients' perception of the value of Art Therapy by people who live with Obsessive Compulsive Disorder (OCD).

In this study, the investigators are proposing to use information from client surveys regarding their experiences in an Art Therapy group within an intensive OCD treatment program, regarding their experience and opinions about the benefits of Art Therapy within a structured, intensive program for individuals who live with severe OCD. Therefore, this proposed study would be an entirely new contribution both to the fields of Art Therapy and OCD.

The hypothesis of the study is that individuals with severe Obsessive-Compulsive Disorder participating in an intensive CBT/ERP treatment program will report benefits specific to their experience in Art Therapy sessions within the program.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: group art therapy

Detailed Description

Objective:

To evaluate patients'/clients' perceptions of the value of art therapy as a treatment component in an intensive CBT/ERP program for individuals with severe OCD.

To this end, survey responses will be collected from clients in the program and analyzed to identify key benefits of including Art Therapy as a component of their treatment experience.

Study logistics:

All clients in the Intensive Treatment Program are expected to attend all groups, Art Therapy included.

Clients will be informed by staff at the beginning of the program, and by the PI in the first Art Therapy group attended, about the study and will be requested to fill out questionnaires they will receive.

After the first Art Therapy group they will be asked to fill out and submit the first questionnaire. After their last group in the program they will be asked to fill out a final questionnaire.

Those who have already completed the program have submitted completed questionnaires and the data from this will be analyzed retrospectively. The data has been de-identified.

Those who begin the program in June will also be offered a beginning and closing questionnaire, and written consent will be sought to use this data for the prospective part of the study.

Method:

Clients who participate in weekly Art Therapy group will be given one questionnaire to complete after their first art therapy group, and one to complete after their tenth group/tenth week in the program. The questionnaire will be a revised version of the questionnaire that has been given to the clients for the retrospective study data gathering.

Data Analysis:

Clients in an intensive OCD residential/day treatment program - men and women age 18 and up are given two electronic surveys, one at the beginning of their 10-week treatment experience, asking questions pertaining to their experience of Art Therapy after their first session, and at the end of their time in the program, asking them to reflect on their overall experience of Art Therapy in the program.(surveys attached). A descriptive statistical analysis will be used to analyze study data.

Procedures for confidentiality/anonymity:

Participant information will be stored on REDCAP, a confidential and encrypted platform for data collection and storage. All participants will have identifying numbers that are de-linked from their names. This date is password-protected: only the research team will have access to this information.

Study Design

Study Type:
Observational
Anticipated Enrollment :
100 participants
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
Art Therapy in an Intensive OCD Program: Client Perception of Value
Actual Study Start Date :
Mar 23, 2023
Anticipated Primary Completion Date :
Mar 30, 2025
Anticipated Study Completion Date :
Mar 30, 2026

Arms and Interventions

Arm Intervention/Treatment
Adults with OCD

Adults with OCD in an intensive treatment program will participate in weekly Art Therapy sessions during their enrollment in the program. Each group is 1.5 hours long. Each participant will be asked to fill out one survey after their first Art Therapy group, and one at the end of the time in the program. Both surveys pertain to their perceptions of the value of Art Therapy within the program.

Behavioral: group art therapy
Art therapy will be offered in a weekly 1.5 hour group. Clients are provided a prompt and then asked to express their feelings using art, such as drawing/painting/etc.

Outcome Measures

Primary Outcome Measures

  1. Art Therapy Questionnaire [October 2020 - November 2023]

    Acceptability of art therapy as rated by scores on the Art Therapy Questionnaire

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Must have been accepted into and begun the Intensive Treatment Program for OCD at the Thompson Centre, whether participating as a residential or day treatment participant.
Exclusion Criteria:
  • No other patients/clients in the hospital or its outpatient programs will be considered for this study. No-one who is not a patient or client in this program can participate

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sunnybrook Health Sciences Centre Toronto Ontario Canada M4N 3M5

Sponsors and Collaborators

  • Sunnybrook Health Sciences Centre

Investigators

  • Principal Investigator: Linda E Chapman, M.C.A.T., Sunnybrook Health Sciences Centre

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sunnybrook Health Sciences Centre
ClinicalTrials.gov Identifier:
NCT05855902
Other Study ID Numbers:
  • 5341
First Posted:
May 12, 2023
Last Update Posted:
May 12, 2023
Last Verified:
May 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 12, 2023