The Acute Effects of Static and PNF Stretching Exercise With Blood Flow Restriction in Athletes

October 22, 2024 updated by: Ayşe Birsu Topcugil Kırık, Dokuz Eylul University

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

The study aims to examine the acute effects of static and proprioceptive neuromuscular facilitation stretching exercises with blood flow restriction on hamstring flexibility, muscle strength, and single leg hop in athletes. Outcome measures were hip range of motion, isometric and eccentric hamstring muscle strength, and single leg hop distance.

Study Overview

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

Interventional

Enrollment (Actual)

109

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

    • Balcova
      • İzmir, Balcova, Turkey, 35330
        • Dokuz Eylul University, Sports Medicine Department

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

  • Adult

Accepts Healthy Volunteers

Yes

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

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 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

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

Investigators

  • Principal Investigator: Ayse Birsu Topcugil Kirik, MD, Dokuz Eylül University

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)

August 20, 2019

Primary Completion (Actual)

August 25, 2023

Study Completion (Actual)

August 25, 2023

Study Registration Dates

First Submitted

February 19, 2024

First Submitted That Met QC Criteria

October 22, 2024

First Posted (Actual)

October 24, 2024

Study Record Updates

Last Update Posted (Actual)

October 24, 2024

Last Update Submitted That Met QC Criteria

October 22, 2024

Last Verified

October 1, 2024

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)?

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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