Examining the Effectiveness of a Wait List Intervention for the Management of Adolescent Eating Disorders
Primary Purpose
Eating Disorders
Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Psychoeducational Workshop and telephone support
Sponsored by
About this trial
This is an interventional treatment trial for Eating Disorders focused on measuring anorexia nervosa, bulimia nervosa, EDNOS
Eligibility Criteria
Inclusion Criteria:
- medical stability at time of referral
- completed referral to the Eating Disorders Program
Exclusion Criteria:
- patients deemed medically unstable are triaged urgently and not eligible for study inclusion
Sites / Locations
- Children's Hospital of Eastern Ontario
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Waitlist Group
Standard of Care
Arm Description
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.
These patients continue to receive the standard of care while awaiting formal assessment.
Outcomes
Primary Outcome Measures
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
Secondary Outcome Measures
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
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01051375
Brief Title
Examining the Effectiveness of a Wait List Intervention for the Management of Adolescent Eating Disorders
Official Title
Examining the Effectiveness of a Wait List Intervention for the Management of Adolescent Eating Disorders
Study Type
Interventional
2. Study Status
Record Verification Date
May 2016
Overall Recruitment Status
Completed
Study Start Date
December 2009 (undefined)
Primary Completion Date
December 2012 (Actual)
Study Completion Date
December 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Ottawa
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The current application targets patient education and enablement, implementation of best practices, continuity of care, and an improvement model to improve efficiencies by investigating whether a brief targeted intervention prior to the first formal ED assessment is efficacious in altering outcome and treatment course.
Detailed Description
The Eating Disorder Program at the Children's Hospital of Eastern Ontario (CHEO) offers a continuum of treatment options to child and adolescent patients with eating disorders (EDs). Although our own funding has increased in recent years, so too have the number of referrals, which has resulted in lengthy wait times for therapeutic assessments by our team. The current application targets patient education and enablement, implementation of best practices, continuity of care, and an improvement model to improve efficiencies by investigating whether a brief targeted intervention prior to the first formal ED assessment is efficacious in altering outcome and treatment course. It is well known that early recognition and implementation of treatment as soon as possible after the onset of symptoms is protective in eating disorders and leads to better success rates and recovery (APA Treatment Guidelines for EDs). It is hoped that the outcome of this study will influence the way in which centers look to address the ongoing issue of lengthy wait times in hopes of offering cost-effective interventions that ultimately improve patient outcomes. By offering an added level of support to families whose referral has been initiated, we hope to ease the burden of primary care providers and increase their satisfaction as it relates to patient safety concerns and complex case management.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Eating Disorders
Keywords
anorexia nervosa, bulimia nervosa, EDNOS
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
51 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Waitlist Group
Arm Type
Experimental
Arm Description
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.
Arm Title
Standard of Care
Arm Type
No Intervention
Arm Description
These patients continue to receive the standard of care while awaiting formal assessment.
Intervention Type
Behavioral
Intervention Name(s)
Psychoeducational Workshop and telephone support
Intervention Description
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.
Primary Outcome Measure Information:
Title
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
Secondary Outcome Measure Information:
Title
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
10. Eligibility
Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
medical stability at time of referral
completed referral to the Eating Disorders Program
Exclusion Criteria:
patients deemed medically unstable are triaged urgently and not eligible for study inclusion
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark Norris, MD
Organizational Affiliation
CHEO
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Wendy Spettigue, MD
Organizational Affiliation
CHEO
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Hospital of Eastern Ontario
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1H 8L1
Country
Canada
12. IPD Sharing Statement
Learn more about this trial
Examining the Effectiveness of a Wait List Intervention for the Management of Adolescent Eating Disorders
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