- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01943734
The Influence of Health Information in Stretch Break Program Participant's Lifestyle
September 16, 2013 updated by: Caroline de Oliveira Martins, Federal University of Paraíba
The Influence of Health Information in Stretch Break Program Participant's Lifestyle: a Quantitative and Qualitative Study
Objective: To verify the influence of information passed during anthropometric assessment would have in physical exercise (PhE) and eating habits of 14 participants (female=11; 51,07+-8,17 years) from the Stretch Break Program of Federal University of Paraíba (SBP of FUPb).
Methods: The research was a descriptive cross-sectional quantitative and qualitative approach.
Were applied, between March and May of 2010, anthropometric evaluation and semi-structured interviews.
During the evaluation were provided information and guidance on health.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
14
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
28 years to 63 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- FUPb white collar workers of either gender
Exclusion Criteria:
- Anyone who did not complete anthropometric measurements
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Lifestyle counseling
Information passed on anthropometric assessment
|
Information passed on worker's anthropometric assessment.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Anthropometric evaluation
Time Frame: Up to 6 weeks
|
Height (cm) was measured with a stadiometer (Sanny), body weight (kg) was measured using a digital scale (TechLine), circumference (cm) was measured (Sanny) at the midpoint between lower costal margin and the superior iliac crest and blood pressure (mmHg) was measured with a sphygmomanometer and a stethoscope (Premium).
Direct measurement assessed body mass index, waist-to-height-ratio and blood pressure classification (determined by highest blood pressure category - systolic blood pressure or diastolic blood pressure).
|
Up to 6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Caroline Martins, PhD, Federal University of Paraíba
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2010
Primary Completion (Actual)
March 1, 2010
Study Completion (Actual)
May 1, 2010
Study Registration Dates
First Submitted
September 10, 2013
First Submitted That Met QC Criteria
September 16, 2013
First Posted (Estimate)
September 17, 2013
Study Record Updates
Last Update Posted (Estimate)
September 17, 2013
Last Update Submitted That Met QC Criteria
September 16, 2013
Last Verified
September 1, 2013
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- CEPHULW298/09
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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