Evaluating the effectiveness of a short video series for social media ("Warna-Warni Waktu") to improve body image among young Indonesian women

ISRCTN ISRCTN35483207
DOI https://doi.org/10.1186/ISRCTN35483207
ClinicalTrials.gov number NCT05023213
Secondary identifying numbers PRR1-10.2196/33596
Submission date
11/04/2022
Registration date
27/04/2022
Last edited
04/04/2023
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Mental and Behavioural Disorders
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data

Plain English Summary

Background and study aims
Body dissatisfaction is a global issue, especially among girls and women. Programmes to help reduce body dissatisfaction exist primarily in higher-income countries, such as the United Kingdom, the United States, and Australia. However, body dissatisfaction is a problem for adolescent and young women in Indonesia, but no local and culturally appropriate programmes or tools exist to address it. The aim of this study is to evaluate the effectiveness of "Warna-Warni Waktu" (WWW), a fictional six-video series with activities that is designed to improve body satisfaction amongst Indonesian young women that will be shared on social media.

Who can participate?
Indonesian girls and young women between the ages of 15 and 19 years can participate. They need to have their own mobile phone and already access Facebook or Instagram every day. They cannot participate if they follow Girl Effect (Springster) on social media or have previously accessed the Springster website. Parental consent is required for those 15-17 years.

What does the study involve?
The study involves 2000 young Indonesian women. At the beginning of the study (Day 1), all participants complete online questionnaires that assess their body satisfaction, how important they think beauty standards are, mood, and satisfaction with their their skin shade. Then, on Day 2, they are randomly split into two groups: half of them are chosen to engage with WWW and half them are not. On Day 3, the group chosen to engage with WWW receives a link every day for six consecutive days (Days 3-8) that includes a WWW video (4-5 minutes long) and its activities (1-5 short activities). Before and after each video, participants are asked one question about their body satisfaction and one question about their mood. On Days 9 and Days 36, both groups complete the same online questionnaires. On Day 37, all participants receive a certificate of participation and a document explaining the purpose of the study, that also includes contact for mental health support. The group that did not engage with WWW, receive a link to access WWW's videos and activities.

What are the possible benefits and risks of participating?
During the development of the video series, Indonesian girls and young women between 15-19 years found the videos to be entertaining and helpful, so participants may have the same positive experience. Participants may also benefit from having the opportunity to share how they feel in a safe and confidential way. The researchers do not foresee or anticipate any significant risk to participants. If participants require any support during or after watching the videos, participating in the activities, or completing the surveys, they have the contact information of the research team in Indonesia, in addition to information for local mental health resources.

Where is the study run from?
The University of the West of England (UWE Bristol) is managing the study. Researchers at UWE Bristol guide and coordinate with a research agency in Jakarta, Indonesia who recruits participants and shares the links to the questionnaires and WWW. All information shared in the questionnaires comes directly to researchers at UWE Bristol.

When is the study starting and how long is it expected to run for?
October 2019 to December 2021

Who is funding the study?
Unilever (Dove Self-Esteem Project)

Who is the main contact?
Heidi Williamson
heidi3.williamson@uwe.ac.uk

Contact information

Prof Phillippa Diedrichs
Principal Investigator

University of the West of England (UWE Bristol)
Frenchay Campus
Coldharbour Ln
Bristol
BS16 1QY
United Kingdom

ORCiD logoORCID ID 0000-0001-5028-4134
Phone +44 (0)11732 83756
Email phillippa.diedrichs@uwe.ac.uk
Dr Heidi Wiliiamson
Scientific

University of the West of England (UWE Bristol)
Frenchay Campus
Coldharbour Ln
Bristol
BS16 1QY
United Kingdom

ORCiD logoORCID ID 0000-0003-0189-4803
Phone +44 (0)117 328 1572
Email heidi3.williamson@uwe.ac.uk
Ms Sharon Haywood
Public

University of the West of England (UWE Bristol)
Frenchay Campus
Coldharbour Ln
Bristol
BS16 1QY
United Kingdom

ORCiD logoORCID ID 0000-0003-0761-5406
Phone +44 (0)117 32 86224
Email sharon.haywood@uwe.ac.uk

Study information

Study designInterventional two-arm single-masked parallel randomized controlled web-based trial
Primary study designInterventional
Secondary study designRandomised controlled trial
Study setting(s)Internet/virtual
Study typePrevention
Participant information sheet Not available in web format, please use contact details to request a participant information sheet
Scientific titleEvaluating the efficacy of a social media-based intervention ("Warna-Warni Waktu") to reduce body dissatisfaction among young Indonesian women: a parallel randomized controlled trial
Study acronymWWW
Study hypothesis1. Participants randomised to the intervention condition will experience improved body satisfaction, mood, and skin shade satisfaction, and reduced internalisation of appearance ideals at 1-day post-intervention, and 1-month follow-up, relative to the waitlist control condition.
2. Each video in the Warna-Warni Waktu series will elicit immediate state-based improvements in body satisfaction and mood.
3. Greater engagement and adherence to the Warna-Warni Waktu intervention will result in improved body satisfaction, mood, and skin shade satisfaction, and reduced internalisation of appearance ideals. This analysis will be exploratory in nature, depending on participants' engagement and adherence to the intervention during the trial.
Ethics approval(s)Approved 20/05/2021, Research Ethics Admin Team UWE Bristol (Northavon House, Frenchay Campus, Bristol, BS16 1QY, UK; +44 (0)117 32 82872; researchethics@uwe.ac.uk), ref: HAS.21.04.138
ConditionBody dissatisfaction in female adolescents and young Indonesian women
InterventionInterventional two-arm single-masked parallel randomised controlled web-based trial with an intervention group and a waitlist control group; block randomisation is performed with a 1:1 allocation with blocks of 4, 6, and 8. (The datasets given to the statistician are masked to the condition.)

Recruitment
Participants are recruited using a local research agency’s database of previous research participants. Previous participants over the age of 40 are contacted via telephone and screened regarding having a daughter within the eligible age range. If the respondent has more than one daughter in the age range, the one with her date of birth closest to the date of contact is chosen. For eligible daughters between 15-17 years old, the recruiter reads the parental information sheet to the parent. Parents provide verbal consent for the daughter's participation, as well as verification of the parents’ identity and daughter's age through photo IDs. Parents answer questions relating to the family’s socioeconomic status before the recruiter requests to speak to the daughter. Then, the daughter is screened for eligibility and informed verbal assent is obtained. A parental information sheet is sent to the parent via WhatsApp, and written informed parental consent is obtained.

A similar pattern of communication occurs with daughters 18-19 years old. Parents verify the age of the parents and the daughter and respond to questions regarding the family's socio-economic status. The adult daughter provides informed verbal and written consent, in the same manner required of parents of those aged 15-17 years.

Intervention:
The intervention, Warna-Warni Waktu (translation to English: Colourful Time Travel), was developed over a 20-month period, from October 2019 - May 2021. In addition to the close collaboration amongst body image academics, creative agencies, social media specialists, not-for-profit organisations, as well as industry funders, development involved three rounds of feedback from the intervention's target audience. The narrative story told in the six-video series is based on the concept of time travel so as to convey the additive impact of body image concerns to young people. A combination of both animated characters and real people are used.

Four risk factors for the development of body image concerns are relevant: 1) social media and influencers 2) appearance-based comparisons 3) appearance-based teasing, and 4) body talk. Each of these risk factors are targeted in videos two through five, with videos one and six being the introductory and concluding videos. Each video is four to five minutes in length. A number of change techniques (including those based upon psychoeducation and media literacy) are embedded within the videos. Each video is accompanied by one to five short interactive activities, designed to elicit cognitive dissonance.

Procedure:
All participants enter the study (i.e., complete the baseline assessment questionnaire) on the same day (Day 1). Participants receive a data package a day prior to this from the research agency to ensure participants have ample mobile phone data to allow participation in the study. A link to the baseline assessment, hosted on Qualtrics (Qualtrics, Provo, UT), is sent to participants via WhatsApp, along with a unique participant identification number (PIN). Participants are requested to enter the PIN on the first page of the baseline survey, in order to match participant responses over time. Participants have 24 hours to complete the baseline assessment; participants that do not complete the baseline assessment within the first 8 hours are sent a reminder message. Following the 24-hour window, participants who complete the baseline assessment are randomised into one of the two conditions. Participants are alerted on Day 2 to what happens next, depending on which condition each are randomised. Participants randomised to the intervention condition are informed to expect a series of links to be sent over the following six days. Participants in the waitlist control condition are informed that contact is to be made again in one weeks' time to complete a second assessment.

On the third day (Day 3), participants in the intervention condition are sent a unique PIN and a link to the first video in the intervention. Again, participants are requested to enter the unique PIN on the first page of the link. Before watching video one in the Warna-Warni Waktu series, participants complete state measures of body satisfaction and mood. State measures of body satisfaction and mood are asked again, immediately after the video. Next, participants are presented with the reinforcer activities for video one to complete. This process is repeated on Days 4-8, for videos two-six.

On Day 9 of the study, participants in both conditions are sent a link to complete the second assessment. As with the baseline assessment, participants are given 24 hours to complete this assessment, with reminder messages sent to non-completers after the first eight hours. The same process is executed for the third and final assessment, one month later on Day 37.

Following the third assessment, all participants are debriefed on the study aims and provided with additional sources of mental health support, as well as a certificate of participation. Those in the waitlist control condition are provided with a link to the Warna-Warni Waktu video series to watch, if desired.
Intervention typeBehavioural
Primary outcome measureBody esteem (body satisfaction) measured using the Body Esteem Scale for Adolescents & Adults (BESAA) at baseline, post-intervention (1 day after the intervention was completed); follow-up (1 month after the intervention was completed)
Secondary outcome measures1. Internalisation of societal appearance ideals measured using the Sociocultural Attitudes Towards Appearance Questionnaire-3 (SATAQ-3) at baseline, post-intervention (1 day after the intervention was completed); follow-up (1 month after the intervention was completed)
2. Positive and negative affect measured using the Positive and Negative Affect Schedule for Children (PANAS-C) at baseline, post-intervention (1 day after the intervention was completed); follow-up (1 month after the intervention was completed)
3. Skin shade satisfaction measured using a two-item purpose-built measure at baseline, post-intervention (1 day after the intervention was completed); follow-up (1 month after the intervention was completed)
4. State body satisfaction measured using a single 101-point visual analogue scale immediately before and after each of the intervention's videos
5. State mood measured using a single 101-point visual analogue scale immediately before and after each of the intervention's videos
Overall study start date01/10/2019
Overall study end date12/12/2021

Eligibility

Participant type(s)Healthy volunteer
Age groupMixed
SexFemale
Target number of participants2000
Total final enrolment2000
Participant inclusion criteria1. Between 15 and 19 years of age
2. Had their own mobile phone
3. Visited Facebook or Instagram every day
Participant exclusion criteria1. Following the Girl Effect brand (Springster) on social media
2. Had previously accessed the Springster website
3. Did not have written consent from a parent or guardian (if under 18 years of age)
Recruitment start date13/09/2021
Recruitment end date05/11/2021

Locations

Countries of recruitment

  • Indonesia

Study participating centre

Infinity CXT
88 Kasablanka Tower, 18th Floor, Tower A
Kota Kasablanka, Raya kav 88
Jakarta
12870
Indonesia

Sponsor information

University of the West of England
University/education

Frenchay Campus
Coldharbour Ln
Bristol
BS16 1QY
England
United Kingdom

Phone +44 (0)1173286224
Email Leigh.Taylor@uwe.ac.uk
Website http://www.uwe.ac.uk/
ROR logo "ROR" https://ror.org/02nwg5t34

Funders

Funder type

Industry

Unilever (Dove Self-Esteem Project)
Government organisation / For-profit companies (industry)
Alternative name(s)
Unilever Global, Unilever PLC, U
Location
United Kingdom

Results and Publications

Intention to publish date28/02/2023
Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryData sharing statement to be made available at a later date
Publication and dissemination planPlans to submit the trial manuscript to the Journal of Medical Internet Research (JMIR), a high-impact peer-reviewed journal.
(added 04/01/2023)
The trial manuscript has been submitted to the Journal of Medical Internet Research (JMIR), a high-impact peer-reviewed journal, and is currently under review, following a revise and resubmit.
IPD sharing planThe data-sharing plans for the current study are unknown and will be made available at a later date.

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Protocol article 28/01/2022 06/10/2022 Yes No
Results article results 03/04/2023 04/04/2023 Yes No

Editorial Notes

04/04/2023: Publication reference added.
04/01/2023: The following changes were made to the trial record:
1. The intention to publish date was changed from 31/12/2022 to 28/02/2023.
2. The publication and dissemination plan was updated.
10/10/2022: The following changes were made to the trial record:
1. The scientific title was changed from 'Evaluating the effectiveness of a social media-based intervention ("Warna-Warni Waktu") to reduce body dissatisfaction among young Indonesian women: a parallel randomized controlled trial' to ''Evaluating the efficacy of a social media-based intervention ("Warna-Warni Waktu") to reduce body dissatisfaction among young Indonesian women: a parallel randomized controlled trial".
2. The intention to publish date was changed from 01/08/2022 to 31/12/2022.
06/10/2022: Publication reference added.
12/04/2022: Trial's existence confirmed by the Research Ethics Admin Team UWE Bristol.