Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
54 participants
INTERVENTIONAL
2022-02-01
2022-05-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Method: Individuals with active knee extension angle limited to at least 15 degree were included in the study, which was designed as a cross-over. Active Knee Extension test and Sit and Reach Test were performed before and after the interventions for the evaluation of hamstring flexibility. Participants were divided into 3 groups as percussion massage, static stretching and control groups, interventions were made with 3 days intervals and control measurements were taken.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Acute Effects of Different Soft Tissue Techniques on Hamstring Tightness
NCT07260630
Which Technique is More Effective for People With Hamstring Tightness in Terms of Balance, Flexibility, and Performance?
NCT05412199
Effects of Dry Needling, Static Stretching and IASTM in People With Hamstring Muscle Shortness
NCT04118231
The Effects of Instrument-Assisted Soft Tissue Mobilization in Sedentary Individuals With Hamstring Tightness
NCT07091383
Effects of Foam Rolling Prior to PNF Stretching on Hamstring Flexibility and Thigh Skin Temperature in Healthy Subjects
NCT04718363
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
sit and reach test: While sitting in a long sitting position with their knees straight and their bodies upright, the participants were asked to touch the soles of their bare feet to the assessment table. In this position, they were told to reach as far as they could reach on the coffee table with their elbows straight and palms facing the floor. By measuring the distance between the fingertip and the coffee table, those who could reach the table received "0" values, those who could reach beyond the table (+) cm and those who could not reach (-) cm. The best value after two measurements was recorded.
Static stretching procedure: For the static stretching exercise, the participant was asked to lie down in the supine position. The investigator had the dominant side passively flexed the hip to 90 degree, extending the knee to the end that could be tolerated. At the last point, it was waited for 30 seconds and then the hamstring muscle was relaxed and rested for 30 seconds. A total of 5 minutes of application was completed by doing 5 repetitions with 30 seconds of static stretching and 30 seconds of rest in each period.
percussion massage procedure: Hypervolt (Hyperice, California, US) device was applied to the dominant hamstring muscle for 5 minutes at 53 Hz frequency with the "hard ball" head. Semitendinosus and semimembranosus muscles were focused in the first 2.5 minutes of the massage treatment, and the biceps femoris muscle in the second 2.5 minutes. By paying attention to the equal amount of pressure applied throughout the massage, the massage was started from the medial side of the muscle in the first part of the application and the massage was completed by moving the device from distal to proximal and from proximal to distal in a straight line within 20 seconds. While passing to the last 2.5 minutes, the massage device was shifted laterally at the distal end of the muscle, and the application was made from distal to proximal and then distally. Thus, the massage for each muscle was started from the medial and ended laterally.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
CROSSOVER
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
percussion massage group
Applying the hypervolt device to the hamstring muscle with the hard ball head for 5 minutes
percussion massage
percussion massage to the dominant leg hamstring muscle for 5 minutes
static stretching group
Static stretching of the hamstring muscle for 5 minutes
static stretching
Static stretching to the dominant hamstring muscle for 5 minutes
control group
no intervention
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
percussion massage
percussion massage to the dominant leg hamstring muscle for 5 minutes
static stretching
Static stretching to the dominant hamstring muscle for 5 minutes
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* Having neurological problems in the lower extremity and lumbar region
* participate in a similar study within the past year
18 Years
25 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Suleyman Demirel University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Pinar Yasar
research assisstant
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Pinar Yasar, MsC
Role: PRINCIPAL_INVESTIGATOR
Suleyman Demirel University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Faculty of Health Sciences
Isparta, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
72867572-050.01.04-31
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.