Evaluation of Skipping Rope and Informational Pamphlet Among Adolescents in South Africa

NCT06516549 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 700

Last updated 2024-11-22

No results posted yet for this study

Summary

The purpose of the study is to evaluate the impact of providing a skipping rope and informational pamphlet to adolescents aged 10-14 years on their physical activity intentions and behaviors from baseline to 12-month follow-up when compared with adolescents of the same age who are not provided with any intervention. This study comprises a two-arm randomized controlled trial nested within an adolescent cohort, i.e. a 'randomized trial-within-cohort'. The intervention will include providing each participant with a skipping rope and a pamphlet with general instructions for skipping the rope and messages about the importance of physical activity. The investigators hypothesize that adolescents in a South African community who are provided with a skipping rope and an informational pamphlet on physical activity will engage in more physical activity behaviors and will report greater intentions to be physically active at a 12-month follow-up, compared to a control group of adolescents who do not receive the intervention.

Conditions

  • Moderate-vigorous Physical Activity (MVPA)

Interventions

OTHER

Skipping rope and informational pamphlet

The provision of a skipping rope and an informational pamphlet to the intervention arm participants will happen during the participant interview within the overall DASH cohort study. The enumerator conducting the survey interview will provide each participant in the intervention group with a skipping rope and pamphlet and will read a short script explaining how to use the rope, outlining the main benefits of physical activity for adolescents, and asking participants to read the pamphlet in their own time.

Sponsors & Collaborators

  • Harvard School of Public Health (HSPH)

    collaborator OTHER
  • Africa Academy for Public Health

    collaborator OTHER
  • Heidelberg University

    collaborator OTHER
  • Technical University of Munich

    collaborator OTHER
  • USINGA Health and Demographic Surveillance System

    collaborator UNKNOWN
  • University of KwaZulu

    lead OTHER

Principal Investigators

  • Jabulani Ncayiyana, Ph.D. · University of KwaZulu

  • Mosa Moshabela · University of KwaZulu

  • Mary Mwanyika-Sando · Africa Academy of Public Health

  • Michael Laxi · Technical University of Munich

  • Till Bärnighausen · Heidelberg University

  • Jacob Burns · Technical University of Munich

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
10 Years
Max Age
14 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-10-01
Primary Completion
2025-12-30
Completion
2025-12-30

Countries

  • South Africa

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06516549 on ClinicalTrials.gov