Actively Recruiting

Phase Not Applicable
Age: 10Years - 14Years
All Genders
Healthy Volunteers
NCT06516549

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

Led by University of KwaZulu · Updated on 2024-11-22

700

Participants Needed

1

Research Sites

65 weeks

Total Duration

On this page

Sponsors

U

University of KwaZulu

Lead Sponsor

H

Harvard School of Public Health (HSPH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

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

Official Title

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

Who Can Participate

Age: 10Years - 14Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Study participant is between ages 10 and 14 years
  • Parents or guardians provide written informed consent for minors
  • Minor participants provide informed assent
  • Participant is a resident of the study area and plans to stay for the entire study duration
Not Eligible

You will not qualify if you...

  • Participants with physical disabilities that prevent physical activity
  • Participants with cognitive impairments affecting decision-making
  • Participants with communication difficulties
  • Participants reporting suicidal behaviors during baseline data collection

AI-Screening

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Trial Site Locations

Total: 1 location

1

University of KwaZulu-Natal

Durban, KwaZulu-Natal, South Africa, 4091

Actively Recruiting

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Research Team

J

Jabulani Ncayiyana, Ph.D.

CONTACT

E

Elisabetta Ferrero, MPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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