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Inspiring Nutritious Selections and Positive Intentions Regarding Eating and Exercise (INSPIRE)

Virginia Commonwealth University (VCU) logo

Virginia Commonwealth University (VCU)

Status

Completed

Conditions

Eating Disorder
Obesity

Treatments

Behavioral: INSPIRE

Study type

Interventional

Funder types

Other

Identifiers

NCT03317587
HM20011075

Details and patient eligibility

About

The aims of the current study are: 1) to pilot a manualized intervention (INSPIRE - Inspiring Nutritious Selections and Positive Intentions Regarding Eating and Exercise) to determine feasibility and acceptability, and 2) to evaluate the preliminary effectiveness of INSPIRE on physical and psychological variables.

Full description

The purpose of the current study is to implement an evidence-based prevention program to promote positive health behaviors among young adult women. It will be one of the first to intentionally execute a prevention program targeting well-established risk factors for both obesity and eating disorders in this high-risk population. Intervention content focuses on promoting body size diversity and emphasizing positive health and behavior change in order to reduce stigmatization and remain sensitive to weight-related issues. The manual was developed by integrating two successful existing prevention programs and expanding on previous prevention efforts. Specifically, the diversity of beauty ideals were highlighted to enhance relevance among ethnic minority women, and distress tolerance and emotion regulation skills training were included to target the maladaptive coping mechanisms young adults use to manage the stress associated with transitioning to college.

Enrollment

29 patients

Sex

Female

Ages

18 to 25 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Currently enrolled in postsecondary education at Virginia Commonwealth University

Exclusion criteria

  • BMI ≥ 30 kg/m2
  • Meet criteria for eating disorder threshold risk
  • Pregnancy

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

29 participants in 1 patient group

INSPIRE
Experimental group
Treatment:
Behavioral: INSPIRE

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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