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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT00220662
Other study ID # BCM99-0177
Secondary ID
Status Active, not recruiting
Phase Phase 3
First received September 16, 2005
Last updated September 16, 2005
Start date June 2000
Est. completion date June 2006

Study information

Verified date July 2004
Source St. Paul's Hospital, Canada
Contact n/a
Is FDA regulated No
Health authority Canada: Health Canada
Study type Interventional

Clinical Trial Summary

This research examines the efficacy of a 5-session individual psychotherapy intervention designed to enhance readiness and motivation for change in individuals with anorexia nervosa, bulimia nervosa, and eating disorder not otherwise specified.

It is hypothesized that individuals randomly assigned to receive Readiness and Motivation Therapy (RMT) will have higher readiness and motivation scores and improved eating disorder and psychiatric symptomatology following the intervention than individuals assigned to a no-treatment control condition.


Description:

Readiness and motivation for change is a significant concern in the treatment of individuals with eating disorders, as evidenced by frequent treatment drop-out, refusal, and relapse. This research examines the efficacy of a 5-session intervention designed to enhance readiness and motivation for change in individuals with anorexia nervosa. A manualized treatment protocol of Readiness and Motivation therapy (RMT) has been developed. It is hypothesized that individuals randomly assigned to RMT will have improved readiness and motivation for change as assessed using the Readiness and Motivation Interview (RMI) at post-treatment, 3-month, and one-year follow-up than individuals assigned to a no treatment control condition. If RMT proves to be effective, it could be added to the menu of treatment options, to permit for better tailoring of treatment to client readiness for change.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 100
Est. completion date June 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- meet DSM-IV diagnostic criteria for anorexia nervosa, bulimia nervosa, or eating disorder not otherwise specified

Exclusion Criteria:

- acute medical crisis

- acute psychiatric crisis

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Readiness and Motivation Therapy


Locations

Country Name City State
Canada Eating Disorders Program, St. Paul's Hospital 1081 Burrard St. Vancouver British Columbia

Sponsors (1)

Lead Sponsor Collaborator
St. Paul's Hospital, Canada

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Readiness and Motivation Scores Post-treatment and at 3-month and one-year follow-up
Secondary Psychiatric and eating disorder symptom severity Post-treatment and at 3-month and one-year follow-up
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