Eating Disorders Clinical Trial
— WICFASOfficial title:
Implementation of a Waitlist Intervention and Clinical Care Pathway for Families Awaiting Services at McMaster Children's Hospital Eating Disorders Program: A Feasibility Study
NCT number | NCT04812899 |
Other study ID # | 13223 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | July 30, 2021 |
Est. completion date | February 4, 2022 |
Verified date | March 2022 |
Source | McMaster University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The COVID-19 pandemic has resulted in several challenges in service delivery for the eating disorders program at McMaster Children's Hospital. Long waiting lists prior to the pandemic (6-9 month wait time) have been made worse by an interruption in service during the initial stages of the pandemic. New routine assessments were placed on hold for many months, while only the most urgently ill children were seen. This, in combination with a dramatic increase in new referrals has resulted in a long waitlist. Now families are waiting 12-18 months for service. The resulting waitlist is now unmanageable and unsafe. Investigators wish to study the implementation of a waitlist intervention which will educate parents on how to start to renourish their children and interrupt eating disordered behaviors. The intervention will consist of a series of educational videos and a book on how to help their children. It is hoped that this intervention can lessen the need for hospitalization and can change the trajectory of symptoms while waiting for service. A clinical care pathway will also be developed to ensure those waiting receive the most appropriate treatment.
Status | Completed |
Enrollment | 30 |
Est. completion date | February 4, 2022 |
Est. primary completion date | February 4, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 7 Years to 100 Years |
Eligibility | Inclusion Criteria: 1. Parents of a child or adolescent (6-17 years) with an Eating Disorder. 2. Have an access to the internet/computer. 3. Have an access to a weigh scale in their home environment 4. Have the capacity to write, speak and understand English Exclusion Criteria: 1. don't have the capacity to write, speak and understand English 2. don't have access to the internet/computer 3. don't have a child or adolescent with an eating disorder |
Country | Name | City | State |
---|---|---|---|
Canada | McMaster Children's Hospital | Hamilton | Ontario |
Lead Sponsor | Collaborator |
---|---|
McMaster University |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Weight trajectory | Change in weight trajectory will be measured over the time period of 14 weeks, starting from the Baseline till the end of the study at 14 weeks | Weight will be collected weekly (in kgs) for 14 weeks. (6 weeks pre intervention, 2 weeks during intervention and 6 weeks post intervention) | |
Primary | Binge/purge episodes trajectory | Change in trajectory of symptoms (number of binge/purge episodes) will be measured pre and post intervention. | Number of binge/purge episodes will be collected weekly for 14 weeks. (6 weeks pre intervention, 2 weeks during intervention and 6 weeks post intervention) | |
Primary | Length of wait time | Average length of wait time pre and post implementation will be determined by examining wait time in the month prior to implementation for new referrals, compared to the average wait time for new referrals in the month following the completion of the study period | At 14 weeks | |
Primary | Change in number of parents who accepted to participate in the study | In terms of recruitment, the investigators will examine the number of parents agree to participate versus the number of families invited to the study. | Baseline and at 14 weeks | |
Primary | Change in number of parents who remain in the study | In terms of retention, the investigators will compare the number of parents completed the study to the number of parents enrolled. | Baseline and at 14 weeks | |
Secondary | Change in Eating Disorder Questionnaire -parent version | Eating Disorder Examination Questionnaire -parent version (EDE-Q) will measures the severity of the characteristic psychopathology of eating disorders. The EDE-Q yields four subscale scores (Restraint, Eating Concern, Weight Concern, and Shape Concern) and a global score measuring the overall severity of eating disorder psychopathology. | Baseline and at 14 weeks | |
Secondary | Change in Parent Versus Eating Disorder Scale | Parent Versus Eating Disorder Scale (PvEDs) is a self-efficacy tool, specifically focused on parental self-efficacy related to re-feeding their child with an Eating Disorder. | Baseline and at 14 weeks | |
Secondary | Change in Nine Item Avoidant/Restrictive Food Intake disorder screen | Nine Item Avoidant/Restrictive Food Intake disorder screen (NIAS) -Parental version is a 9-item, Likert scale questionnaire that inquires about picky eating, interest in food, and eating habits driven by a fear of negative consequences. Minimum score is 0 and maximum is 45. A score of = 24 is considered a positive ARFID screen. | Baseline and at 14 weeks | |
Secondary | Change in Pediatric Symptom Checklist-17 | Pediatric Symptom Checklist-17 (PSC-17) is a 17-item general mental health screening tool that can help to assess the likelihood of finding any mental health disorder. Minimum score is 0 and maximum is 35. A total score of 15 or more points may indicate the need for a referral to a qualified medical or mental health professional. | Baseline and at 14 weeks | |
Secondary | Change in Carers Needs Assessment Measure | Carers Needs Assessment Measure (CaNAM): This 47 item questionnaire is designed to assess the needs of a carer of someone with an eating disorder. The minimum score is 0, the maximum score is 64. A higher score indicates that the carer has received sufficient information and support for themselves and their child. | Baseline and at 14 weeks |
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