"The Healthy Body Image" (HBI) Program: A Program to Promote a Positive Body Image

March 20, 2024 updated by: Professor Jorunn Sundgot-Borgen, Norwegian School of Sport Sciences

"The Healthy Body Image" (HBI) Program: A Program to Promote a Positive Body Image. A School-based Randomized Controlled Trial

Too many Norwegian adolescents experience severe body dissatisfaction (40-70 %), and strive to accomplish the "perfect body". At the same time, only 50 % meet the government's recommendations on physical activity and intake of fruits and vegetables. Also, 14-24 % has unhealthy sleeping habits. Optimizing these lifestyle factors is associated with physical and psychological health. These factors, along with the pressure to obtain the "perfect" body, are threatening the adolescent's physical and psychological health, jfr. Meld St nr 19. It is now a need for knowledge on how the investigators can contribute to promote positive body experience among the adolescents.

It has recently, through a controlled study on elite youth athletes at Norwegian sports high schools, been shown that it is possible to change eating habits, improve body image and reduce new cases of eating disorder. It is now desirable to test an adapted program through a school-based program at regular Norwegian high school students (12th grade). Today, no controlled, school-based intervention studies with long-term follow-up have been conducted.

The main aim of this project is to investigate if it is possible, through a school-based intervention program (Healthy Body Intervention), to promote positive body image, increase physical activity level, and healthy eating and sleeping habits in both boys and girls at Norwegian high schools.

The intervention program will contribute with new evidence-based knowledge on the effect of an adapted health-promoting program.

Study Overview

Detailed Description

The design is a school-based randomized controlled trial (RCT) intervention, using the methods questionnaire and interview to obtain data. Based on statistical power analyses, all high schools in Oslo and Akershus County will be asked to participate in the study. After the schools have responded, consenting schools will be stratified (by size and geographical affiliation) and randomized to the intervention or the control condition. To minimize contamination biases within schools, the investigators prepare a cluster-randomized design.The population should contain 17-20 schools (1400 students at 2nd year). Data collection is conducted through pre-test and post-test 1, 2, and 3 (acute, 3, and 12 month post-intervention). At post-test 1, a selection is invited to participate in an interview about feasibility in addition to the questionnaire. It is an intervention for students containing interactive lecturers with discussion, team work, discussions and home assignments.

Study Type

Interventional

Enrollment (Actual)

4193

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Oslo, Norway, 0806
        • Norwegian School of Sports Sciences

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years to 19 years (Child, Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Norwegian high schools
  • High schools located in either Oslo or Akershus County
  • Students in the 2nd grade fall 2016
  • Students within academic specialization education programs
  • Teachers teaching included students in Norwegian, Social studies, Physical education, and contact teachers
  • School nurses working at the randomly selected schools
  • School administrators at randomly selected schools

Exclusion Criteria:

  • Schools that follow foreign school systems
  • Students within vocational education programs
  • School departments connected to prison

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Healthy Body Image
Students receive the Healthy Body Image intervention containing 3x90 minutes of interactive workshops with the addition of related homework after each workshop.
Interactive workshops (3 x 90 minutes) include training techniques to increase media literacy, enhance self-esteem, positive body image, awareness of perfectionism, and include discussions related to truths and myths related to life style factors. Homework is an extension of each workshop that is simple and not time-consuming tasks to increase reflection and awareness of how all the mentioned factors are a part of their lives.
Other Names:
  • Healthy Body Image
No Intervention: Control group
Students do not receive the intervention program.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Proximal and distal effect of the "Healthy Body Intervention" (HBI) program on change in positive body image
Time Frame: Participants are asked to complete the questionnaire at post-tests planned at week 1, 3 months and 12 months after intervention
Participants are asked to respond to questions by choosing from different responses presented on a likert scale. Positive body image is assessed by the Experience of Embodiment Scale.
Participants are asked to complete the questionnaire at post-tests planned at week 1, 3 months and 12 months after intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Proximal and distal effect of the HBI program on change in self-esteem
Time Frame: Participants are asked to complete the questionnaire at post-tests planned at week 1, 3 months and 12 months after intervention
Participants are asked to respond to questions by choosing from different responses presented on a likert scale. The scale used is the Rosenberg Self-esteem scale.
Participants are asked to complete the questionnaire at post-tests planned at week 1, 3 months and 12 months after intervention
Proximal and distal effect of the "Healthy Body Intervention" (HBI) program on change in the prevalence of students meeting the recommendations for health promoting physical activity.
Time Frame: Participants are asked to complete the questionnaire at post-tests planned at week 1, 3 months and 12 months after intervention
The outcome will be measured through a self-developed Physical Activity level/habit questionnaire, including choosing a specific response on a likert scale and response through open ended questions.
Participants are asked to complete the questionnaire at post-tests planned at week 1, 3 months and 12 months after intervention
Experience of the intervention program and the feasibility of running the HBI program in schools.
Time Frame: Post-test is planned within first week after intervention
To measure the outcome, a self-developed interview guide in addition to a self-developed questionnaire asking students and school staff about the experience of the intervention program and the feasibility of the intervention. When answering the questionnaire, participants are asked to respond by choosing a response on a likert scale.
Post-test is planned within first week after intervention
Proximal and distal effect of the HBI program on change in eating behavior (nutrition intake
Time Frame: Participants are asked to complete the questionnaire at post-tests planned at week 1, 3 months and 12 months after intervention
The outcome will be measured through a self-developed Food frequency questionnaire where responses are chosen from a likert scale.
Participants are asked to complete the questionnaire at post-tests planned at week 1, 3 months and 12 months after intervention
Proximal and distal effect of the HBI program on change in sleeping quality and sleep patterns
Time Frame: Participants are asked to complete the questionnaire at post-tests planned at week 1, 3 months and 12 months after intervention
The outcome is measured through The Bergen Insomnia Scale, 6 items and 3 items assessing delayed sleep phase and by asking the participants (using a likert scale) how many hours of sleep they usually get per night during a normal weekday and a weekend day.
Participants are asked to complete the questionnaire at post-tests planned at week 1, 3 months and 12 months after intervention
Proximal and distal effect of the HBI program on change in academic achievements
Time Frame: Participants are asked to complete the questions included in the questionnaire package at post-tests planned at week 1, 3 months and 12 months after intervention
Participants are asked to choose the correct grade they received on their last report card, from a scale presenting the possible grades.
Participants are asked to complete the questions included in the questionnaire package at post-tests planned at week 1, 3 months and 12 months after intervention
Proximal and distal effect of the "Healthy Body Intervention" (HBI) program on change in health related quality of life
Time Frame: Participants are asked to complete the questionnaire containing all the below presented measures at post-tests planned at week 1, 3 months and 12 months after intervention
Participants are asked to respond to questions by choosing from different responses presented on a likert scale. Health related quality of life will be assessed through the "Screening for and Promotion of Health Related Quality of Life in Children an Adolescents - a European Public Health Perspective - 10" (KIDSKREEN-10).
Participants are asked to complete the questionnaire containing all the below presented measures at post-tests planned at week 1, 3 months and 12 months after intervention
Proximal and distal effect of the HBI program on change in symptoms of eating disorders
Time Frame: Participants are asked to complete the questionnaire at post-tests planned at week 1, 3 months and 12 months after intervention
Symptoms of eating disorders is assessed by the Eating Disorder Examination Questionnaire - 11 (EDE-Q 11)
Participants are asked to complete the questionnaire at post-tests planned at week 1, 3 months and 12 months after intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 1, 2016

Primary Completion (Actual)

February 1, 2018

Study Completion (Actual)

February 1, 2018

Study Registration Dates

First Submitted

April 24, 2016

First Submitted That Met QC Criteria

September 10, 2016

First Posted (Estimated)

September 15, 2016

Study Record Updates

Last Update Posted (Actual)

March 21, 2024

Last Update Submitted That Met QC Criteria

March 20, 2024

Last Verified

August 1, 2021

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • JCSB

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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