Effects of a school-based health intervention programme in Port Elizabeth, South Africa: The KaziBantu project
- Conditions
- The planned study will provide basic insights regarding the efficacy and effectiveness of school-based health promotion measures to increase children’s and teachers’ health and health-related behaviours.Not Applicable
- Registration Number
- ISRCTN18485542
- Lead Sponsor
- ovartis Foundation
- Brief Summary
2017 Results article in http://dx.doi.org/10.4081/gh.2017.601 results 2018 Results article in http://dx.doi.org/doi.org/10.1371/journal.pntd.0006332 results 2018 Results article in https://pubmed.ncbi.nlm.nih.gov/29626554/ results 2018 Results article in http://dx.doi.org/10.1371/journal.pone.0206908 results 2019 Results article in http://dx.doi.org/10.3390/ijerph16020232 results 2019 Protocol article in https://www.ncbi.nlm.nih.gov/pubmed/31298224 protocol (added 15/07/2019)
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 1120
Children:
1. Grade 1-6
2. Aged 6-14 years
3. Written informed consent by parent/guardian
4. Not participating in other clinical trials
5. Not suffering from medical conditions that prevent participation in physical activity
Teachers:
1. Involved in implementation of the school-based health promotion programme
2. Tick all questions with yes in the Physical Activity Readiness Questionnaire to be able to take part in the cardiorespiratory fitness test
Children:
1. Suffering severe malnourishment (as diagnosed by a study nurse following national guidelines. In this case, children will be referred to local clinics)
Teachers:
1. Acute or chronic medical conditions that prevent participation in a submaximal fitness test (if uncertain, participant will be asked to consult a general practitioner and provide a doctor's certification before he/she is included in the study)
2. Temporary illness such as a cold or fever (to participate in cardiorespiratory fitness test)
3. Minimum 50% employment rate for at least 6 months
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method