- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06656858
The Acute Effects of Static and PNF Stretching Exercise With Blood Flow Restriction in Athletes
The Acute Effects of Static and PNF Stretching Exercise With Blood Flow Restriction on Hamstring Flexibility, Muscle Strength and Single Leg Hop in Athletes : A Randomized Controlled Trial
Study Overview
Status
Conditions
Detailed Description
A total of 109 athletes were included in the study. Participants were randomized into five groups: (1) static stretching, (2) proprioceptive neuromuscular facilitation (PNF) stretching, (3) blood flow restriction (BFR) + static stretching, (4) BFR + PNF stretching, and (5) control groups. Stretching exercises were performed on the dominant leg hamstring muscle group for 3 sets of 15 seconds each. BFR was applied during the stretching to the blood flow restriction (BFR) + static stretching and BFR + PNF stretching groups. No stretching was applied to the control group.
Assessments were performed at baseline and immediately after stretching. Hamstring flexibility (hip joint range of motion) was assessed via the passive straight leg raise test. Isometric and eccentric hamstring muscle strength were measured using a hand-held dynamometer, and muscle power was assessed using the single leg hop distance.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Balcova
-
İzmir, Balcova, Turkey, 35330
- Dokuz Eylul University, Sports Medicine Department
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age between 18-40 years old
- Engaged in regular physical activity for at least 8 hours a week for the last 6 months
- Body mass index (BMI) < than 30 kg/m²
- Momentary blood pressure less than 135/85 mmHg
Exclusion Criteria:
- History of fractures or surgical operations involving the lower limbs, hips, or lumbar region
- history of fractures, surgeries and other diagnosed medical conditions on the lower extremity, hip, and lumbar region
- Systemic musculoskeletal disease
- Pain in the lower back, hips, or lower extremities
- Known hip deformity or diagnosis of scoliosis
- History of deep vein thrombosis or embolism
- Diagnosis of circulatory system diseases such as hypertension or peripheral vascular disease
- History of anemia
- Previous cerebrovascular disease or myocardial infarction.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Static stretching
Static stretching exercises were performed on the dominant leg's hamstring muscle group for 3 sets of 15 seconds.
|
Static stretching exercises were performed on the dominant leg's hamstring muscle group for 3 sets of 15 seconds
|
|
Active Comparator: PNF stretching
PNF stretching exercises were performed on the dominant leg's hamstring muscle group for 3 sets of 15 seconds.
|
PNF stretching exercises were performed on the dominant leg's hamstring muscle group for 3 sets of 15 seconds.
|
|
Experimental: Static stretching with BFR
Static stretching exercises were performed on the dominant leg's hamstring muscle group for 3 sets of 15 seconds with BFR application.
|
Static stretching exercises were performed on the dominant leg's hamstring muscle group for 3 sets of 15 seconds with BFR application.
|
|
Experimental: PNF stretching with BFR
PNF stretching exercises were performed on the dominant leg's hamstring muscle group for 3 sets of 15 seconds with BFR application
|
PNF stretching exercises were performed on the dominant leg's hamstring muscle group for 3 sets of 15 seconds with BFR application.
|
|
Other: Control
No stretching was applied to the control group.
An information brochure about hamstring injuries was provided to the participants.
|
No stretching was applied to the control group.
An information brochure about hamstring injuries was provided to the participants.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
hamstring flexibility
Time Frame: immediately after intervention
|
Passive straight leg rise test for dominant leg
|
immediately after intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Power
Time Frame: immediately after intervention
|
single leg hop distance for dominant and non-dominant leg
|
immediately after intervention
|
|
muscle strength
Time Frame: immediately after intervention
|
isometric and eccentric hamstring muscle strength of the dominant leg
|
immediately after intervention
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ayse Birsu Topcugil Kirik, MD, Dokuz Eylül University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 5016-GOA
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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