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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

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

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04686864
Enrollment
36
Registered
2020-12-29
Start date
2021-01-21
Completion date
2022-01-21
Last updated
2022-09-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Eating Disorders

Keywords

eating disorder, parent support group

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.

Interventions

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.

Sponsors

McMaster University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

We studied the implementation of a virtual parent-led peer support group.

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
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

Design outcomes

Primary

MeasureTime frameDescription
Change in number of parents who remain in the support groupBaseline and 6 months laterWe 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.
Number of support groups each parent attends6 months after baselineWe will take note of how many support groups the parent attends in a 6 month period.
Cost12 months after baselineTo assess cost, we will collect data on the costs of the technology, software, and time (of parents and the facilitator).

Secondary

MeasureTime frameDescription
Change in Carer BurdenBaseline, 3 months, 6 monthsCarer 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).
Change in Carer NeedsBaseline, 3 months, 6 monthsCarer 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.
Change in Parental Self Efficacy and CollaborationBaseline, 3 months, 6 monthsParental 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.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026