A Virtual Parent-led Support Group for Parents of Children and Youth With Eating Disorders: A Mixed Methods Feasibility Study Examining Acceptability, Cost and Parent Outcomes

Sponsor
McMaster University (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT04686864
Collaborator
(none)
40
1
1
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Study Details

Study Description

Brief Summary

There is a gap in the literature about the feasibility and implementation of parent-led support groups for parents who have children or adolescents with eating disorders. In this study, we will be observing the experiences of 40 parents in Ontario who will virtually participate in one of 3 parent-led support groups for parents of children and youth with eating disorders. Parents will be expected to attend the virtual sessions twice a month over the course of six months. We hope to evaluate the acceptability, cost, and parental outcomes of the parent-led support groups via surveys before, during, and after the study, as well as using a post-study interview.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Support Group for Caregivers
Early Phase 1

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
A Virtual Parent-led Support Group for Parents of Children and Youth With Eating Disorders: A Mixed Methods Feasibility Study Examining Acceptability, Cost and Parent Outcomes
Actual Study Start Date :
Jan 21, 2021
Anticipated Primary Completion Date :
Dec 1, 2021
Anticipated Study Completion Date :
Dec 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Parent Support Group

Support and psychoeducation in a group setting for parents who have a child or adolescent with an eating disorder.

Behavioral: Support Group for Caregivers
Engage parents in the community via this support group, so they can be supported by other parents who "know the system", can advise them on how to proceed, and empower them to help their children. Parents will learn psychoeducation about eating disorders and how to support their children.

Outcome Measures

Primary Outcome Measures

  1. Change in number of parents who remain in the support group [Baseline and 6 months later]

    We will compare the number of parents who initially sign up for the support group to how many parents have stayed in the support group 6 months later.

  2. Number of support groups each parent attends [6 months after baseline]

    We will take note of how many support groups the parent attends in a 6 month period.

  3. Cost [12 months after baseline]

    To assess cost, we will collect data on the costs of the technology, software, and time (of parents and the facilitator).

Secondary Outcome Measures

  1. Change in Carer Burden [Baseline, 3 months, 6 months]

    Carer Burden will be assessed using the Eating Disorders Symptom Impact Scale (EDSIS) - a 24 item measure examining the impact of symptoms on parents' lives. Minimum score is 0, maximum score is 96. A higher score indicates that the child's eating disorder symptoms are having a greater impact on their parent (more burdensome).

  2. Change in Carer Needs [Baseline, 3 months, 6 months]

    Carer Needs will be assessed using the Carers Needs Assessment Measure (CaNAM), a 47-item questionnaire examining information received about eating disorders, support received from other people and organizations, support for self, and areas where help is needed. 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.

  3. Change in Parental Self Efficacy and Collaboration [Baseline, 3 months, 6 months]

    Parental self-efficacy and collaboration will be assessed using the Patient and Carer Collaboration Scale -C (PACCS), a 33-item questionnaire examining constructs such as hope, self-care and compassion, externalization of the eating disorder, and boundaries. Each question is evaluated on a scale of 0 to 100, where higher values indicate positive collaboration with their child and higher parental self efficacy.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 100 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • have the capacity to write, speak and understand English, in order to participate in the sessions

  • have access to the internet/computer to participate in the sessions

  • must have a child or adolescent with an eating disorder.

Exclusion Criteria:
  • don't have the capacity to write, speak and understand English

  • don't have access to the internet/computer

  • don't have a child or adolescent with an eating disorder

Contacts and Locations

Locations

Site City State Country Postal Code
1 McMaster University Hamilton Ontario Canada L8N3Z5

Sponsors and Collaborators

  • McMaster University

Investigators

  • Principal Investigator: Jennifer Couturier, MD MSc, McMaster University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jennifer Couturier, Dr. Jennifer Couturier, McMaster University
ClinicalTrials.gov Identifier:
NCT04686864
Other Study ID Numbers:
  • 12703
First Posted:
Dec 29, 2020
Last Update Posted:
Nov 2, 2021
Last Verified:
Oct 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Jennifer Couturier, Dr. Jennifer Couturier, McMaster University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 2, 2021