Body Image Clinical Trial
Official title:
Evaluating "Dove Confident Me Indonesia"; A School-Based Single Session Intervention to Improve Body Image and Wellbeing Among Indonesian Adolescents
Verified date | July 2023 |
Source | University of the West of England |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Negative body image is an important public health concern for young people due to its prevalence and detrimental impact on young people's health, education, and social life. Encouragingly, a number of interventions have been designed to improve adolescent body image in school settings, with promising results. However, the vast majority of studies testing these interventions are conducted in high-income, English speaking countries, despite increasingly recognition that negative body image is a global concern. As such, it is important to develop and disseminate interventions to foster positive body image among adolescents in low-to-middle income countries, too. Research indicates high prevalence rates of negative body image among adolescents in many Asian countries. Indonesia - the focus of the present research - is an emerging middle-income country in South East Asia. A recent U-Report Poll (UNICEF, 2020) found almost 80% of the young people surveyed wanted to change something about their appearance, suggesting a degree of body dissatisfaction and approximately 50% stopped themselves from doing something that was important to them because of appearance concerns. Moreover, according to the same poll, over 90% of Indonesian adolescents surveyed reported to wanting to learn ways to improve their body image in school or online. To date, no body image interventions have been adapted and trialled in Indonesia. Therefore, this project aims to evaluate the effectiveness as well as the acceptability and feasibility of a specially adapted version of Dove Confident Me Single Session among Indonesian adolescents that will be integrated into UNICEF's Life Skills Education curriculum. Notably, the session has been designed to be feasible to deliver in low-resource schools (e.g., that do not access to the internet or facilities to show videos or PowerPoint slides). To assess the acceptability, feasibility, and effectiveness of the intervention, the study will compare the body image and well-being of students who take part in the programme to students who do not take part in any programme (classes as usual). Investigators will also gather in-depth feedback from students, and teachers via focus groups and surveys, in order to inform future improvement of the programme for wider implementation. To undertake this project, the investigators will recruit students and teachers from approximately 10 state junior secondary schools in Indonesia via a local research agency. Students will complete questionnaire assessments of body image and well-being before and after programme period, and again 8 weeks later to assess longer-term benefits. COVID response: In light of the ongoing pandemic, some research activities will take place online. Decisions on delivery format (online / in-person / hybrid) were made on the basis of continued risk assessments and considerations of local government guidelines.
Status | Completed |
Enrollment | 1926 |
Est. completion date | July 1, 2022 |
Est. primary completion date | April 4, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 11 Years to 15 Years |
Eligibility | Inclusion Criteria: - All participating schools must be state junior secondary schools. - Students in grade 7 through 9 are eligible. - Students must speak Bahasa Indonesia and must have moderate-high literacy. levels in Bahasa Indonesia - i.e., need to be able to read on their own. - Students must have access to a device with online access (e.g., laptop or iPad). Exclusion Criteria: - Non-Bahasa Indonesia speaking students. - Religious or private schools. |
Country | Name | City | State |
---|---|---|---|
United Kingdom | Centre for Appearance Research, UWE | Bristol |
Lead Sponsor | Collaborator |
---|---|
University of the West of England | Indonesia University, UNICEF, Unilever R&D, University of Hawaii |
United Kingdom,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in body esteem | Body esteem will be assessed using the weight and appearance evaluation subscales of the Body Esteem Scale for Adolescents & Adults (BESAA, Mendelson, Mendelson & White, 2001). Responses to the 18 items are on a 5-point Likert-type scale. Once the appropriate items are reverse coded, scores will be averaged with higher scores indicating higher body esteem. | Baseline; post intervention (1 week after the intervention) and follow-up (8 weeks after the intervention). | |
Secondary | Change in internalisation of societal appearance ideals | Internalisation of societal appearance ideals will be assessed using the general subscale of the Sociocultural Attitudes Towards Appearance Questionnaire-3 (SATAQ-3; Thompson, Van Den Berg, Roehrig, Guarda, & Heinberg, 2004). Scores will be averaged with higher scores indicating higher internalisation. Mean score range = 1-5. | Baseline; post intervention (1 week after the intervention) and follow-up (8 weeks after the intervention). | |
Secondary | Change in mood | Positive and negative affect will be measured using the Positive and Negative Affect Schedule (Crawford & Henry, 2004). Scores on each subscale will be averaged; with higher scores indicating greater negative affect and positive affect respectively. Mean score range for each subscale = 1-5. | Baseline; post intervention (1 week after the intervention) and follow-up (8 weeks after the intervention). | |
Secondary | Change in tendency to engage in appearance comparisons | Two purpose-built items will assess participants' tendency to engage in appearance comparisons. Responses to both items will be on a 5-point Likert-type scale (1=Never to 5=Often). Scores will be averaged with higher scores indicating a greater tendency to engage in appearance comparisons. | Baseline; post intervention (1 week after the intervention) and follow-up (8 weeks after the intervention). | |
Secondary | Skin shade satisfaction | Three purpose-built items will assess participants' satisfaction with their skin shade (i.e., the precise colour of their skin). Responses to the initial two items will be on a 5-point Likert-type scale.
'How dissatisfied or satisfied you are with the colour of your skin?' is rated from 1=very dissatisfied to 5 = very satisfied. 'Which of the following statements do you agree with the most' - 1 = I would like my skin colour to be lighter, 2 = I would like my skin colour to stay the same and 3 = I would like my skin colour to be darker. The final skin shade satisfaction item will use a visual representation of skin colours (1=darkest skin shade to 9=lightest skin shade). Participants will be asked which skin shade is most alike to their current skin colour, and then which skin shade is closest to their 'ideal' skin colour. |
Baseline; post intervention (1 week after the intervention) and follow-up (8 weeks after the intervention) |
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