- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00638924
Physiologic Variables in Healthy Women in Shuttle Walk Test
June 13, 2012 updated by: Juliana Gomes Z|abatiero, University of Campinas, Brazil
Analysis of Physiologic Variables in Healthy Women in Shuttle Walk Test
To analyze the alterations of physiologic variables in healthy sedentary women in the Shuttle Walk Test, verify the distance reached and interruption causes of the test.
Study Overview
Detailed Description
The Shuttle Walk Test requires patients to walk at a gradually increasing speed, up and down a 10 meter corridor identified by two marker cones, until they reach a symptom limited maximum.
The walking speed was externally paced and controlled by a series of beeps played on a compact disk.
Study Type
Observational
Enrollment (Actual)
40
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
São Paulo
-
Campinas, São Paulo, Brazil, 13083887
- State University of Campinas
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-
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
20 years to 30 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Sampling Method
Non-Probability Sample
Study Population
women, between 20 and 30 years old, healthy and sedentary
Description
Inclusion criteria:
- female gender;
- sedentary;
- aged 20 to 30 years.
Exclusion criteria:
- pregnancy;
- enrolment in any regular physical activity program;
- diagnosed health conditions.
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Exercise Capacity
Individuals from the female gender; age range of 20 to 30 years old; considered healthy (i.e. with no diagnosed health condition; considered sedentary (i.e.
performing less than 150 minutes of moderate intensity physical activity per week); will be asked to volunteer in the research and perform a exercise capacity test.
|
the test requires patients to walk at a gradually increasing speed, up and down a 10 m course identified by two marker cones, until they reach a symptom limited maximum.
The walking speed was externally paced and controlled by a series of beeps played on a compact disk.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Shuttle Walk Test Distance
Time Frame: baseline
|
The distance achieved in the test in meters
|
baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Heart Rate
Time Frame: baseline
|
Heart rate at baseline
|
baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Ivete Alonso Saad, dr, University of Campinas, Brazil
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
December 1, 2007
Primary Completion (Actual)
February 1, 2008
Study Completion (Actual)
February 1, 2008
Study Registration Dates
First Submitted
March 12, 2008
First Submitted That Met QC Criteria
March 12, 2008
First Posted (Estimate)
March 19, 2008
Study Record Updates
Last Update Posted (Estimate)
July 17, 2012
Last Update Submitted That Met QC Criteria
June 13, 2012
Last Verified
June 1, 2012
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 200802
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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