ClinicalTrials.Veeva

Menu

Feasibility and Acceptability of a Single Session of Imagery Rescripting in a Community Sample of Adults

University of Oregon logo

University of Oregon

Status and phase

Completed
Early Phase 1

Conditions

Depressive Symptoms
Acceptability
Disordered Eating Behaviors
Feasibility Studies

Treatments

Behavioral: imagery rescripting
Behavioral: nutrition education

Study type

Interventional

Funder types

Other

Identifiers

NCT06610318
STUDY00000529

Details and patient eligibility

About

Negative experiences related to eating and appearance (NEREAs), such as critical commentary from parents about food, are common. They are also associated with depression and disordered eating, predictors of early mortality. Imagery rescripting (IR) is a therapeutic process during which individuals are guided through recalling distressing memories, like NEREAs, and generating ideas for bringing support into these memories. Single sessions of IR demonstrate promise in shifting the primary negative consequences of NEREAs in clinical samples of women. The current study examined the feasibility and acceptability of a remote-delivered, single session of IR in a community sample of men and women with NEREAs.

Enrollment

27 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. ≥18 years old
  2. endorse a history of at least one negative experience related to eating and/or appearance

Exclusion criteria

  1. endorsed a current major medical condition;
  2. met criteria for a full threshold psychiatric disorder (of moderate intensity when severity ratings are necessary, such as for substance use disorders and binge eating disorder);
  3. were at high risk for suicide;
  4. endorsed current or recent pregnancy or anticipated becoming pregnant within the next year;
  5. were taking medication known to affect eating, weight and/or chronic disease risk;
  6. were participating in eating, weight, or diabetes programming;
  7. experienced weight loss > 10% in the past six months; and/or
  8. could not complete study procedures in English.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

27 participants in 2 patient groups

Imagery rescripting
Experimental group
Description:
This condition has three stages. In the first stage, participants were asked to select their most distressing memory related to their appearance (not physical or sexual trauma). They were asked to visualize the selected memory, in detail, as if it were happening to them again. Then, interventionists used a downward arrow technique to identify two-to-three maladaptive core schema. In the second stage, participants were asked to identify a real or imagined trusted adult. Then, they were asked to imagine what their younger self might need to cope with or feel calmer in the situation of their selected memory. In the third stage, the participant was instructed to imagine asking the trusted adult for what they need and to imagine the trusted adult providing their selected interventions and describe how they feel afterwards. These procedures were then repeated with participants' most distressing memory related to eating. This session was remote delivered via Zoom.
Treatment:
Behavioral: imagery rescripting
Nutrition education control
Active Comparator group
Description:
The active control condition consisted of a time- and attention-matched general nutrition education session. The curriculum for this intervention included information from the United States Department of Agriculture's Dietary Guidelines (e.g., food labels, describing the benefits of macronutrients). This session was remote delivered using Zoom.
Treatment:
Behavioral: nutrition education

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems