- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03384264
Effect of Suspension Training in the Elderly
December 23, 2017 updated by: Francesco Campa
Changes in Phase Angle and Handgrip Strength Induced by Suspension Training in Older Women: A Randomized Controlled Trial
This study aimed to analyze the effects of a 12-week suspension exercise training programme on handgrip strength (HG) and anthropometric and bioelectrical impedance parameters in older adults.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
30
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
60 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
non-hypertensive and not receiving hormonal replacement therapy,
Exclusion Criteria:
performing any regular physical exercise more than once a week over the 6 months preceding the beginning of the study
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: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: TG
|
The suspension device was securely attached to a fixed beam.
The suspension programme included an initial 10 min warm-up with very low-intensity joint mobility exercises.
The central part of the program had a duration of 40 min and included six exercises in which the level of intensity was based on the inclination of the body.
The exercises were performed in a split routine, alternating by segment to prevent joint overload.
Finally, participants performed 10 minutes of stretching.
|
No Intervention: CG
the CG maintained their normal physical activity habits over the study
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Phase angle
Time Frame: 12 weeks
|
Bioelectrical impedance parameter
|
12 weeks
|
Body composition
Time Frame: 12 weeks
|
anthropometric measures
|
12 weeks
|
Handgrip strength
Time Frame: 12 weeks
|
strength
|
12 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Actual)
January 1, 2017
Primary Completion (Actual)
January 12, 2017
Study Completion (Actual)
April 1, 2017
Study Registration Dates
First Submitted
December 19, 2017
First Submitted That Met QC Criteria
December 23, 2017
First Posted (Actual)
December 27, 2017
Study Record Updates
Last Update Posted (Actual)
December 27, 2017
Last Update Submitted That Met QC Criteria
December 23, 2017
Last Verified
December 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- 28102016
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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