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

Status

Unknown

Conditions

Intervention / Treatment

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

Study Locations

      • 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.

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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