Data from: Effectiveness of tailored multichannel interventions on weight loss among adolescents: A Randomized controlled trial
Data files
Mar 26, 2026 version files 198.76 KB
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2_months_assessment.csv
57.16 KB
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5_months_assessment.csv
57.16 KB
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baseline_assessment.csv
59.98 KB
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information_sheet.csv
18.96 KB
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README.md
5.50 KB
Abstract
Overweight among adolescents is a public health issue. However, several weight loss interventions were developed and conducted for adolescents. These interventions are often not adequately tailored to the needs of this vulnerable target group. Besides, these interventions proposed that one channel is adequate to deliver the message to adolescents. The proposed study aims to evaluate the effectiveness of tailored multichannel interventions on weight loss among adolescents. The proposed study is a prospective, randomized controlled trial. 279 adolescents were recruited from 8 non-medical colleges in Mansoura University. For intervention participants, the tailored intervention is designed and guided by a health belief model and takes into account evidence-based recommendations. The intervention was designed by a multidisciplinary team and administered by 10 nurses for 5 months, including five face-to-face school meetings, five school-based telephone calls, and five WhatsApp text messages. Control group participants received 2 non-tailored face-to-face sessions. The primary outcome is the mean difference in weight loss between groups. The proposed study hypothesizes that the participants who receive tailored multichannel intervention lose significantly more weight (Body Mass Index) compared with the control group. Secondary outcomes include a health belief model.
Dataset DOI: 10.5061/dryad.sj3tx96k5
Description of the data and file structure
Dataset Title: Weight Management Intervention Study – Baseline, 2-Month, and 5-Month Follow-Up Data
1. General Description
This dataset contains participant-level data from a weight management intervention study conducted among university students. Data were collected at three time points:
- Baseline (pre-intervention)
- 2 months post-intervention
- 5 months post-intervention
The dataset includes demographic characteristics, anthropometric measures, and questionnaire-based variables derived from health belief model constructs, self-efficacy scales, and behavioral assessments related to diet and physical activity.
All data are anonymized. Participants are identified only by unique study codes.
2. File Structure
The dataset contains four files:
- information_sheet.csv
- baseline_assessment.csv
- 2_months_assessment.csv
- 5_months_assessment.csv
a. information sheet
This sheet contains variable descriptions and coding schemes for categorical variables.
It provides:
- Variable names
- Variable Description
- Variable codes
b. baseline
Contains baseline (pre-intervention) data for all participants.
Includes:
- Anthropometric measures
- Health belief model constructs
c. 2 months
Contains follow-up data collected 2 months after intervention.
Includes:
- Anthropometric measures (weight, height, and BMI)
- Health belief model constructs
d. 5 months
Contains follow-up data collected 5 months after intervention.
Includes:
- Anthropometric measures
- Health belief model constructs
Health Belief Model Constructs
The key constructs of the HBM include 89 statements. 13 questions assessed perceived severity, 7 questions assessed perceived susceptibility, 14 questions addressed perceived barriers, 13 questions on perceived benefits, 12 questions on cues to action, 18 questions evaluated self-efficacy in dieting, 7 questions on self-efficacy in exercise, and 5 questions on the behavioral intention of weight management (dieting and exercising). All items are self-reported and scored on a 5-point Likert scale, with 1 representing "strongly disagree" and 5 indicating "strongly agree.” Higher scores denoted a more positive belief toward overweight preventive behaviors.
A. Perceived Severity
- Emotional severity:
severityEM1–severityEM4 - Physical severity:
severityPHY5–severityPHY9 - Social severity:
severitySOC10–severitySOC13
B. Perceived Susceptibility
- Lifestyle susceptibility:
susceptLifestyle1–susceptLifestyle5 - Environmental susceptibility:
susceptEnv6–susceptEnv7
C. Perceived Barriers
- Practical barriers:
barrierPractic1–barrierPractic4 - Emotional barriers:
barrierEmot5–barrierEmot9 - Awareness barriers:
barrierAware10–barrierAware14
D. Perceived Benefits
- Emotional benefits:
BenefitsEmot1–BenefitsEmot4 - Physical benefits:
BenefitsPhys5–BenefitsPhys11 - Social benefits:
BenefitsSocial12–BenefitsSocial13
E. Cues to Action
- Internal cues:
CuesInt1–CuesInt6 - External cues:
CuesExt7–CuesExt12
F. Self-Efficacy Measures
Dietary Habit Self-Efficacy
EfficacydietHabit1–EfficacydietHabit13
Emotional Eating Self-Efficacy
EfficacydietEmot14–EfficacydietEmot18
Exercise Self-Efficacy
EfficacyExercise1–EfficacyExercise7
Higher scores indicate greater perceived self-efficacy.
G. Behavioral Outcomes
Dietary Behavior
BehavDiet1BehavDiet2BehavDiet3
Exercise Behavior
BehavExercises4BehavExercises5
Human subjects data
All data included in this dataset was collected in accordance with applicable ethical standards for research involving human participants. Prior to data collection, ethical approval was obtained from the appropriate institutional review board (IRB), and all participants provided informed consent to participate in the study. As part of the consent process, participants were explicitly informed that their data may be shared in a fully de-identified form for research and publication purposes, including deposition in a public data repository.
To ensure participant privacy and confidentiality, the dataset has been thoroughly de-identified prior to submission. All direct identifiers have been removed, including names, student identification numbers, contact information, and any other uniquely identifying personal details. Indirect identifiers that could potentially enable re-identification (such as highly specific demographic or contextual variables) have been carefully reviewed and either generalized, recoded, or excluded where necessary.
Participants are represented only by anonymized study codes that cannot be traced back to individual identities. No linkage file or key connecting participant identities to study codes is included in this dataset or retained in any publicly accessible location.
The dataset has been reviewed to ensure compliance with relevant data protection and privacy regulations and follows best practices for anonymization of human subjects' data. The authors confirm that the data, in its current form, poses minimal risk of re-identification and is suitable for sharing in the public domain.
Study design: Randomized controlled trial
Inclusion Criteria:
- Students in the first and second grades of college whose body mass index (BMI) of 25 or higher at the baseline assessment will be eligible to participate in the study.
Exclusion Criteria:
- Students will be excluded if they have one of the following criteria.
- Students who report a physical condition or chronic illness or impairment preventing them from being physically active
- Students who have physical conditions that prevent them from losing excess body weight
- Students who are on medication that causes weight gain
- Students with a history of mental health disorders
- Students participating in another weight loss program
Primary Purpose : Supportive Care
Allocation : Randomized
Interventional Model : Parallel Assignment
Interventional Model Description: prospective, open label, barreled two groups. The study participants will be assigned randomly to intervention group or control group. The participants in the intervention group will receive the tailored Multichannel Interventions, while the control group will receive two supportive sessions. The intervention group will not receive the tailored multichannel intervention.
Masking: None (Open Label)
Primary Outcome Measures
BMI: Weight in kg and height in cm will be assessed. BMI will be measured, calculated, and interpreted based on WHO guidelines and using BMI charts. Overweight is considered when a BMI is 25 kg/m2 and Obesity is equivalent to a BMI of 30 kg/m2 or over (WHO, 2024).
Secondary Outcome Measures
Health belief model construct: The key constructs of the HBM include 89 statements.(Jones et al., 2015) (Albasheer et al., 2024). Each statement will be rated on a 5-point Likert scale, ranging from 1 (strongly disagree) to 5 (strongly agree). 13 questions evaluated perceived severity on three subscales (emotional/mental, health, physical health/fitness, and social professional). 7 questions evaluated perceived susceptibility and consisted of two subscales (lifestyle and environmental). 14 questions dealt with perceived barriers, comprising three subscales (practical concerns, emotional/mental health, and awareness). 13 questions on perceived benefits included three subscales (emotional/mental health, physical health/fitness, and social/professional). The 12 questions on cues to action consisted of two subscales (internal and external cues to action). 18 questions assessed self-efficacy in dieting and included two subscales (habits, preferences and emotional/mental health). The 7 questions on self-efficacy in exercise.
Data collection:
All data related to primary and secondary outcomes will be collected at baseline (T0) at 2 (T1) months, and 5 months (T2) after the start of intervention.
