- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05113719
Effect of Bridge Exercise Performed at Different Knee Angles
November 24, 2021 updated by: Fettah Saygılı, Gazi University
Investigation of the Effect of Bridge Exercise Performed at Different Knee Angles on Muscle Strength and Endurance in Healthy Cases
Stabilization exercises help increase strength, stability, balance, gait, and endurance through effective abdominal training.
Bridge exercise, which is one of the closed kinetic exercises, is one of the most used spinal stabilization exercises.
Although that exercise affects on the trunk muscles, it has been stated that it is related to all muscles of the lower extremity.There are some studies, which are examining the activation of the gluteus maximus, quadriceps, rectus abdominus, iliocostalis lumborum, iliocostalis thoracis, and gastrocnemius muscles while exercising the bridge.
Although there are some studies investigating the activation of muscles at different knee angles, there is no study in the literature examining the effect of bridge exercise performed at different knee angles on the strength and endurance of lower extremity and trunk muscles.
For these reasons, this study aimed to examine the effect of bridging exercises performed at different knee angles on muscle strength and endurance in healthy subjects.
Study Overview
Detailed Description
Participants included in the study will randomly divide into 3 different groups by using simple sealed envelope randomization method.
Participants in the first group will perform exercise at knee angle was 45⁰ flexion, the participants in the second group will perform to exercise at knee angle 60⁰ flexion and the participants in the third group will perform exercise knee angle at 90⁰ flexion.
All participants will include in a bridging exercise program by a blind researcher at predetermined knee angles (45⁰, 60⁰ 90⁰), 3 sets of 15 repetitions per day, 3 days a week for 6 weeks.
Evaluations will be done by a blinded researcher 1 week before starting the 6-week exercise program and 1 week after they finished the program.
All evaluations will be made by the same physiotherapist by meeting with participants face to face.
Inclusion in the research will be on a voluntary basis.
As outcome measures, muscle strength assessment and core Endurance Assessment will be evaluated.
Study Type
Interventional
Enrollment (Actual)
45
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
-
-
-
Denizli, Turkey
- Pamukkale University
-
-
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 27 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Being between the ages of 18-27
- Not having any health problems diagnosed in terms of starting the exercise program
- Individuals who do not exercise regularly
Exclusion Criteria:
- Having any identified health problem that would prevent the exercise
- Individuals who exercise regularly
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Bridge exercise at knee angle 45 degree
The group will perform the bridge exercise at a 45-degree knee flexion angle.
|
Both groups will perform bridge exercise
|
|
Experimental: Bridge exercise at knee angle 60 degree
The group will perform the bridge exercise at a 60-degree knee flexion angle.
|
Both groups will perform bridge exercise
|
|
Experimental: Bridge exercise at knee angle 90 degree
The group will perform the bridge exercise at a 90-degree knee flexion angle.
|
Both groups will perform bridge exercise
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscle Strength Assessment-Baseline
Time Frame: Assessment will be conducted before intervention.
|
PowerTrack II Command will be used.
The back extensor muscle group and M. Gluteus Maximus, M. Quadriceps Femoris, M. Gastrocinemius muscles of the participants will be evaluated.
|
Assessment will be conducted before intervention.
|
|
Muscle Strength Assessment-Post intervention
Time Frame: Assessment will be conducted immediately after the intervention.
|
PowerTrack II Command will be used.
The back extensor muscle group and M. Gluteus Maximus, M. Quadriceps Femoris, M. Gastrocinemius muscles of the participants will be evaluated.
|
Assessment will be conducted immediately after the intervention.
|
|
Abdominal Muscle Strength Assessment-Baseline
Time Frame: Assessment will be conducted before intervention.
|
Manual Muscle Test will be used.
|
Assessment will be conducted before intervention.
|
|
Abdominal Muscle Strength Assessment-Post intervention
Time Frame: Assessment will be conducted immediately after the intervention.
|
Manual Muscle Test will be used.
|
Assessment will be conducted immediately after the intervention.
|
|
Core Endurance Assessment-1-Baseline
Time Frame: Assessment will be conducted before intervention.
|
Prone Plank Endurance Test
|
Assessment will be conducted before intervention.
|
|
Core Endurance Assessment-1-Post intervention
Time Frame: Assessment will be conducted immediately after the intervention.
|
Prone Plank Endurance Test
|
Assessment will be conducted immediately after the intervention.
|
|
Core Endurance Assessment-2-Baseline
Time Frame: Assessment will be conducted before intervention.
|
Squat Endurance Test
|
Assessment will be conducted before intervention.
|
|
Core Endurance Assessment-2-Post intervention
Time Frame: Assessment will be conducted immediately after the intervention.
|
Squat Endurance Test
|
Assessment will be conducted immediately after the intervention.
|
|
Core Endurance Assessment-3-Baseline
Time Frame: Assessment will be conducted before intervention.
|
Dynamic Abdominal Endurance Test
|
Assessment will be conducted before intervention.
|
|
Core Endurance Assessment-3-Post intervention
Time Frame: Assessment will be conducted immediately after the intervention.
|
Dynamic Abdominal Endurance Test
|
Assessment will be conducted immediately after the intervention.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Study Chair: Fettah SAYGILI, PT, M.Sc., Research assistant
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.
Helpful Links
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)
July 1, 2020
Primary Completion (Actual)
July 1, 2021
Study Completion (Actual)
October 10, 2021
Study Registration Dates
First Submitted
October 28, 2021
First Submitted That Met QC Criteria
October 28, 2021
First Posted (Actual)
November 9, 2021
Study Record Updates
Last Update Posted (Actual)
December 8, 2021
Last Update Submitted That Met QC Criteria
November 24, 2021
Last Verified
November 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- 1-Brige Exercise
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
There is no plan to make IPD data but when the statistical analysis of all data is made, all results will be shared.
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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