Examining the Effectiveness of a Wait List Intervention for the Management of Adolescent Eating Disorders
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|ClinicalTrials.gov Identifier: NCT01051375|
Recruitment Status : Completed
First Posted : January 18, 2010
Last Update Posted : May 12, 2016
|Condition or disease||Intervention/treatment||Phase|
|Eating Disorders||Behavioral: Psychoeducational Workshop and telephone support||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||51 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||Examining the Effectiveness of a Wait List Intervention for the Management of Adolescent Eating Disorders|
|Study Start Date :||December 2009|
|Actual Primary Completion Date :||December 2012|
|Actual Study Completion Date :||December 2012|
Experimental: Waitlist Group
The intervention involves completion of a single workshop, provision of psychoeducational materials, and regular telephone support with a specially trained nurse-coordinator to parents of youth on our waiting list, within a month of our receiving the referral.
Behavioral: Psychoeducational Workshop and telephone support
The intervention involves completion of a single workshop (delivered by a psychiatrist and adolescent health physician), provision of psycho educational materials, and regular telephone support with a specially trained nurse-coordinator to parents of youth on our waiting list.
No Intervention: Standard of Care
These patients continue to receive the standard of care while awaiting formal assessment.
- Investigate whether a wait list intervention for patients and families who are on a wait list, improves patient presentation at the time of formal assessment, as well as 6-months post-assessment [ Time Frame: 18 months ]
- Evaluate the impact that a wait list intervention group workshop has on caregiver knowledge, stress, and self-efficacy pertaining to eating disorders and their treatment [ Time Frame: 12 months ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01051375
|Children's Hospital of Eastern Ontario|
|Ottawa, Ontario, Canada, K1H 8L1|
|Principal Investigator:||Mark Norris, MD||CHEO|
|Principal Investigator:||Wendy Spettigue, MD||CHEO|