- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02307357
The Effects of Newcomball Training on Physical Fitness and Mood State of Middle Age Women in Israel
December 1, 2014 updated by: Hillel Yaffe Medical Center
Habitual physical activity was found to be positively related to better health and well-being.
One of the most popular physical activity forms is ball games.
In Israel, there is a growing popularity in a new ball game - Newcomball - which is being played by many middle age, non-athlete, women.
However, so far, no study had evaluated the contribution of the game to improvement in the participants' physical fitness.
The aim of this study, therefore, is to evaluate the effects of six month two weekly Newcomball training sessions to the physical fitness of middle age women.
Study Overview
Detailed Description
Physical fitness will be evaluated by six different physical tests: 1. agility T test, 2. "shuttle run" test for aerobic capacity, 3. vertical jump, 4. power ball throw, 5. "sit and reach" flexibility test , 6. 20 m all-out run speed test.
Study Type
Interventional
Enrollment (Anticipated)
120
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: sharon tsuk, PhD
- Phone Number: 972-9-8639235
- Email: sharontsuk1@gmail.com
Study Locations
-
-
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Netanya, Israel
- Wingate Institute
-
-
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 50 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- healthy adults women
Exclusion Criteria:
non healthy, using drugs, competitive athletes women-
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: Diagnostic
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: newcomball players
active newcomball women players will perform physical fitness tests
|
the subjects will perform 6 different tests to evaluate their physical fitness
|
Experimental: control
not physically active women will perform physical fitness tests
|
the subjects will perform 6 different tests to evaluate their physical fitness
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Evaluation of physical fitness of newcomball players vs. non active women
Time Frame: six month
|
we will perform physical fitness tests to 2 groups: newcomball players and non active women in the beginning of games season and in the middle of the season.
the measure is:.vertical jump, measured by power plate (in seconds),
|
six month
|
Evaluation of physical fitness of newcomball players vs. non active women
Time Frame: six month
|
power ball through measures the distance in meters
|
six month
|
Evaluation of physical fitness of newcomball players vs. non active women
Time Frame: six month
|
agility T-test, measures time to complete the test( in seconds)
|
six month
|
Evaluation of physical fitness of newcomball players vs. non active women
Time Frame: six month
|
flexibility measures the distance of hands in a sit and reach test (centimeters)
|
six month
|
Evaluation of physical fitness of newcomball players vs. non active women
Time Frame: six month
|
velocity measures time to complete 20 meters run (seconds)
|
six month
|
Evaluation of physical fitness of newcomball players vs. non active women
Time Frame: six month
|
aerobic shuttle run test, measures the time and distance completed in graded run test, in which velocity increased until exhaustion (meter and minutes)
|
six month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Study Director: sharon tsuk, PhD, Wingate Institute
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, 2014
Primary Completion (Anticipated)
August 1, 2016
Study Completion (Anticipated)
August 1, 2016
Study Registration Dates
First Submitted
November 6, 2014
First Submitted That Met QC Criteria
December 1, 2014
First Posted (Estimate)
December 4, 2014
Study Record Updates
Last Update Posted (Estimate)
December 4, 2014
Last Update Submitted That Met QC Criteria
December 1, 2014
Last Verified
December 1, 2014
More Information
Terms related to this study
Other Study ID Numbers
- 0056-14
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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