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Cognitive Behavioural Therapy-Ten for Eating Disorders

N/A
Waitlist Available
Led By Elizabeth Phoenix
Research Sponsored by Lawson Health Research Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up pre-treatment; post-treatment (on average 10 weeks for cbt-t and 25 weeks for cbt-e) 3, 6, 12, 24 months post treatment. treatment is on average 10 weeks for cbt-t and 25 weeks for cbt-e
Awards & highlights

Summary

This trial will compare two types of cognitive behavioural therapy for people with eating disorders who are not underweight. The goal is to see which therapy is more effective and has less drop-out.

Eligible Conditions
  • Eating Disorders

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~pre-treatment; post-treatment (on average 10 weeks for cbt-t and 25 weeks for cbt-e) 3, 6, 12, 24 months post treatment. treatment is on average 10 weeks for cbt-t and 25 weeks for cbt-e
This trial's timeline: 3 weeks for screening, Varies for treatment, and pre-treatment; post-treatment (on average 10 weeks for cbt-t and 25 weeks for cbt-e) 3, 6, 12, 24 months post treatment. treatment is on average 10 weeks for cbt-t and 25 weeks for cbt-e for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change in Eating Disorder Cognitions
Change in the frequency of Binge Eating
Change in the frequency of Vomiting
Secondary study objectives
Binge Eating Change over the Course of Treatment
Change in Depression symptoms
Change in Impulsivity
+6 more

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: CBT-TExperimental Treatment1 Intervention
Participants will be randomly assigned to one of two conditions (CBT-E or CBT-T). Participants who agree to participate will receive 10 weeks of CBT-T.
Group II: CBT-EActive Control1 Intervention
Participants will be randomly assigned to one of two conditions (CBT-E or CBT-T). CBT-E will occur over the course of 25 weeks and be delivered as it typically is in the clinic setting of the investigators.

Find a Location

Who is running the clinical trial?

Lawson Health Research InstituteLead Sponsor
672 Previous Clinical Trials
414,451 Total Patients Enrolled
University of Western Ontario, CanadaOTHER
164 Previous Clinical Trials
319,178 Total Patients Enrolled
Elizabeth PhoenixPrincipal InvestigatorLondon Health Sciences Centre
~14 spots leftby Sep 2025
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