Trunk Extension Endurance Among Physical Therapy Students

May 20, 2020 updated by: Tarek Mohamed El-gohary, General Committee of Teaching Hospitals and Institutes, Egypt

Trunk Extension Endurance Using Four Arms Positions Among Physical Therapy Collegiate Students

College students from physical therapy department will be assigned into four groups. Participants will be tested for trunk extensors endurance and will be given endurance training program to do at home for 6 to 8 weeks. Spinal mobility and lower extremity mobility will be measured. Isokinetic outcome measures for extension and flexion at two different speeds will also be measured at baseline, after 6 and 8 weeks.

Study Overview

Status

Completed

Conditions

Detailed Description

Active physical therapy students who are healthy and free from any significant pain at the spine will be recruited to participate in intervention endurance training. Participants will be assigned into four equal groups; doing trunk extension form lying on stomach while breathing normally and arching trunk backwards as long as tolerated. Group one will have arms above head, group two will have hands behind head, group three will have hands parallel to the trunk, and group four will receive instructions only and will act as control group. Spinal mobility of forward bending, backwards bending, right and left side bending will be taken. Straight leg raising and quadriceps flexibility will also be taken. Isokinetic measurements including peak torque, peak torque/body weight, average peak torque, work and average power will be taken at baseline, 6 and 8 weeks. Participants will have a training volume of 2 sets of 10 repetitions, 2 minutes rest in between, 2x/day for 6 to 8 weeks. Endurance timing will be measured in seconds using stop watch. If participant managed to maintain the trunk extension position for 4 minutes, time is recorded and it is considered as ceiling time.

Study Type

Interventional

Enrollment (Actual)

52

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 Locations

      • Al Madīnah, Saudi Arabia, 20012
        • College of medical rehabilitation sciences

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

18 years to 25 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • Active college student free from any spinal pain or pain 3/10 on pain intensity numeric pain rating scale, willing to participate

Exclusion Criteria:

  • have had spinal surgery or pain at the spine more than 3/10 on pain intensity numeric pain rating scale.

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: PREVENTION
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: DOUBLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
ACTIVE_COMPARATOR: trunk endurance with hands above head
participants had to practice trunk extensors endurance training with having hands above head.
endurance training
Other Names:
  • trunk endurance
ACTIVE_COMPARATOR: trunk endurance with hands behind head
participants had to practice trunk extensors endurance training with having hands behind head.
endurance training
Other Names:
  • trunk endurance
ACTIVE_COMPARATOR: trunk endurance with hands parallel
participants had to practice trunk extensors endurance training with having hands parallel to the trunk.
endurance training
Other Names:
  • trunk endurance
NO_INTERVENTION: trunk endurance with no intervention
participants will be tested for trunk extensors endurance with having hands on chest but no intervention.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
endurance timing
Time Frame: 8 weeks
trunk extensors endurance timing
8 weeks
isokinetic output
Time Frame: 8 weeks
peak torque, peak torque/BW, average peak torque, average power, work
8 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Tarek M El-gohary, PhD, Taibah University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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)

February 20, 2017

Primary Completion (ACTUAL)

November 20, 2017

Study Completion (ACTUAL)

December 31, 2017

Study Registration Dates

First Submitted

April 5, 2017

First Submitted That Met QC Criteria

April 10, 2017

First Posted (ACTUAL)

April 11, 2017

Study Record Updates

Last Update Posted (ACTUAL)

May 22, 2020

Last Update Submitted That Met QC Criteria

May 20, 2020

Last Verified

May 1, 2020

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • CMR-PT-2017-01

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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