NCT06843200

Brief Summary

This clinical trial is evaluating the effects of a 2-hour, small group discussion with parents and caregivers of adolescents in Oregon. We 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. We will also evaluate whether the children of these parents/caregivers experience improvements in their disordered eating and mood symptoms.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
240

participants targeted

Target at P75+ for not_applicable

Timeline
1mo left

Started Jan 2025

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress90%
Jan 2025Jul 2026

Study Start

First participant enrolled

January 27, 2025

Completed
3 days until next milestone

First Submitted

Initial submission to the registry

January 30, 2025

Completed
25 days until next milestone

First Posted

Study publicly available on registry

February 24, 2025

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2026

Last Updated

February 24, 2025

Status Verified

January 1, 2025

Enrollment Period

1.4 years

First QC Date

January 30, 2025

Last Update Submit

February 18, 2025

Conditions

Outcome Measures

Primary Outcomes (9)

  • Parent/caregiver disordered eating symptoms

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

    baseline to 1-month

  • Parent-child feeding practices

    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).

    baseline to 1-month

  • Parent/caregiver weight bias internalization

    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).

    baseline to 1-month

  • Exercise avoidance

    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).

    baseline to 1-month

  • Parent/caregiver self-compassion

    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.

    baseline and 1-month

  • Parent/child body ideal internalization

    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).

    baseline and 1-month

  • Parent/caregiver stress

    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).

    baseline and 1-month

  • Parent/caregiver fat talk

    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).

    baseline and 1-month

  • Parent/caregiver anti-fat attitudes

    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).

    baseline and 1-month

Secondary Outcomes (8)

  • child disordered eating symptoms

    baseline to 1-month

  • Parent-child relationship (child report)

    baseline to 1-month

  • child anti-fat bias

    baseline to 1-month

  • Child exercise avoidance

    baseline to 1-month

  • fat talk (child report of parent/caregiver)

    baseline and 1-month

  • +3 more secondary outcomes

Study Arms (2)

Intervention

EXPERIMENTAL

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

Behavioral: Parent Group Discussion

Wait-list control

NO INTERVENTION

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

Interventions

A 2-hour interactive parent group delivered to 5-10 parents via zoom; discuss weight bias and discrimination; brainstorm ways to respond in parent-child interactions involving health and appearance; and identify action steps.

Intervention

Eligibility Criteria

Age12 Years+
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • 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
  • years of age
  • can read and understand English at the 6th grade level or higher

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Oregon

Eugene, Oregon, 97405, United States

RECRUITING

MeSH Terms

Conditions

Disordered Eating BehaviorDepressionFeeding Behavior

Condition Hierarchy (Ancestors)

BehaviorFeeding and Eating DisordersMental DisordersBehavioral SymptomsBehavior, Animal

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 30, 2025

First Posted

February 24, 2025

Study Start

January 27, 2025

Primary Completion (Estimated)

July 1, 2026

Study Completion (Estimated)

July 1, 2026

Last Updated

February 24, 2025

Record last verified: 2025-01

Data Sharing

IPD Sharing
Will not share

Locations