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NCT03125993
Effects of Brisk Walking on Overweight/Obesity Population
NA trial testing >10000 steps brisk walking in Obesity in 150 participants. Status unknown.
25 August 2017
Quick facts
| Lead sponsor | Guangdong Center for Disease Prevention and Control |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | prevention |
| Enrollment | 150 |
| Start date | 25 April 2017 |
| Primary completion | 25 August 2017 |
| Estimated completion | 30 August 2017 |
Drugs / interventions tested
- >10000 steps brisk walking
Conditions studied
- Obesity — all drugs for Obesity →
Sponsor
Guangdong Center for Disease Prevention and Control
Who can join
Eligibility, any sex, with Obesity. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
1.Objective The investigators aim to determine the effect of brisk walking prescription (\> 10000 steps, \> five days, per week) on body components and metabolic risk factors among patients with overweight/obesity. The objectives are as follow: 1. The body components changes before/after the brisk walking prescription (\> 10000 steps, \> five days per week) intervention in overweight/obesity population; 2. The metabolic risk factors changes before/after the brisk walking prescription (\<10000 steps or \<five days per week) intervention in overweight/obesity population 2.Study design This study is a prospective 4-month follow-up scheme in which patients were treated with the following intervention: \> 10000 steps, \> five days, per week. For individual follow-up, body components and metabolic risk factors will be tested before and after the study. Every participants will be followed up in community visits every month. 3\. Statistical analysis Statistical analysis will be performed using SPSS 16.0 version package (SPSS Inc., Chicago, IL.). Numerical data will be presented as mean ± standard deviation for normal distribution or otherwise median (interquartile range). Two-sided independent t-test is adopted for between-group comparison on end-points with normal distribution, otherwise non-parametric test. Row-Column table will be analyzed through chi-square test. P\<0.05 is taken as statistical significant.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
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- PubMed search for NCT03125993
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03125993 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Guangdong Center for Disease Prevention and Control
- Last refreshed: 24 April 2017
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