Skip to main content
Clinical Trials/NCT06843200
NCT06843200Active, not recruitingNot Applicable

Conversations With Caregivers About Health and Appearance

University of Oregon1 site in 1 country112 target enrollmentStarted: January 27, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
112
Locations
1
Primary Endpoint
Parent/caregiver disordered eating symptoms

Study Overview

Brief Summary

This clinical trial is evaluating the effects of a 2-hour, small group discussion with parents and caregivers of adolescents in Oregon. The investigators will evaluate whether parents'/caregivers' experience reductions in their disordered eating symptoms, mood symptoms, and parent-child relationship quality, relative to parent/caregiver participants in the wait list control. The investigators will also evaluate whether the children of these parents/caregivers experience improvements in their disordered eating and mood symptoms.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Single (Participant)

Eligibility Criteria

Ages
12 Years to — (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •for parent/caregiver:
  • •at least 18 years old
  • •the primary caregiver of at least one child 12-17 years old who lives with them at least 50% of the time
  • •living in the state of Oregon
  • •can read and understand English at the 6th grade level or higher
  • •access to internet and private space for zoom
  • •Inclusion criteria for the child:
  • •12-17 years of age
  • •can read and understand English at the 6th grade level or higher

Exclusion Criteria

  • Not provided

Arms & Interventions

Wait-list control

No Intervention

wait-list control group will receive the same intervention after data collection ends

Intervention

Experimental

a single 2-hour, remote delivered interactive group parenting session

Intervention: Parent Group Discussion (Behavioral)

Outcomes

Primary Outcomes

Parent/caregiver disordered eating symptoms

Time Frame: baseline to 1-month

Disordered eating will be measured using the 36-item Eating Disorder Examination Questionnaire (EDE-Q)

Parent-child feeding practices

Time Frame: baseline to 1-month

Child feeding practices will be assessed using the modified Comprehensive Feeding Practices Questionnaire (CFPQ). The monitoring, restriction for weight, restriction for health, environment, modeling, and teaching about nutrition subscales (27-items) will be used. 4 responses on the measure are rated on a 5-point scale from 1 (never) to 5 (always), while the rest are rated on a 5-point scale from 1 (disagree) to 5 (agree).

Parent/caregiver weight bias internalization

Time Frame: baseline to 1-month

Weight bias internalization will be measured using the modified 10-item Weight Bias Internalization Scale (WBIS-M). Responses on the measure are rated on a 7-point scale from 1 (strongly disagree) to 7 (strongly agree).

Exercise avoidance

Time Frame: baseline to 1-month

Exercise avoidance will be assessed using 2-items used in previous research (More et al., 2019). Responses on the measure are rated on a 7-point scale from 1 (not at all true) to 7 (completely true).

Parent/caregiver self-compassion

Time Frame: baseline and 1-month

Self-compassion will be assessed using the 12-item Self-Compassion Scale-Short Form (SCS-SF). Responses on the measure are rated on a 5-point scale from 1 (almost never) to 5 (almost always). Higher summed scores indicate greater self-compassion. The SCS-SF has near perfect correlation with the original 26-item Self-Compassion Scale.

Parent/child body ideal internalization

Time Frame: baseline and 1-month

Sociocultural attitudes towards appearance, including thin-ideal internalization, muscular-ideal internalization, and appearance-related pressures will be measured using three subscales from the Sociocultural Attitudes Towards Appearance Questionnaire Revised-3 (SATAQ-R). The Internalization-TV/Mag, Internalization-Athlete, and Internalization-Comparison subscales (13-items) subscales will be used. Responses on the measures are rated on a 5-point scale from 1 (definitely disagree) to 5 (definitely agree).

Parent/caregiver stress

Time Frame: baseline and 1-month

Parental stress will be measured using the 18-item Parental Stress Scale (PSS). Responses on the measure are rated on a 5-point scale from 1 (strongly disagree) to 5 (strongly agree).

Parent/caregiver fat talk

Time Frame: baseline and 1-month

Frequency of fat talk will be assessed using the 16-item Family Fat Talk Questionnaire. Responses on the measure are rated on a 5-point scale from 1 (never) to 5 (always).

Parent/caregiver anti-fat attitudes

Time Frame: baseline and 1-month

Anti-Fat attitude will be assessed using 3-items from the Willpower subscale of the Anti-Fat Attitudes Questionnaire (AFA). Responses on the measure are rated on a 9-point scale from 0 (very strongly disagree) to 9 (very strongly agree).

Secondary Outcomes

  • Parent-child relationship (child report)(baseline to 1-month)
  • child anti-fat bias(baseline to 1-month)
  • Child exercise avoidance(baseline to 1-month)
  • child disordered eating symptoms(baseline to 1-month)
  • fat talk (child report of parent/caregiver)(baseline and 1-month)
  • child weight bias internalization(baseline and 1-month)
  • child body ideals internalizations(baseline and 1-month)
  • child self-compassion(baseline and 1-month)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials