Effects of Different Electrophysical Agents in Hamstring Muscles Flexibility of Healthy Individuals

NCT04328155 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2021-03-10

No results posted yet for this study

Summary

Sixty healthy individuals will be randomised into four groups. Group I (15 subjects) will be applied hotpacks, Group II (15 subjects) will be applied infrared, Group III will be applied ultrasound to hamstring muscles for 18 sessions 3 times per week and the subjects will do hamstring self stretching exercise 3 times for 15 seconds. Group IV will only do self stretching exercises.

Outcome measures are Range of Motion and hamstring flexibility. Measurements will record before and after the end of the treatment.

Conditions

  • Flexibility
  • Hamstring Muscles

Interventions

PROCEDURE

Hotpack Group

Hotpack Group received 20 minutes hotpack to hamstring muscles region at prone position and participants stretched the hamstring muscles at supine position.Self stretching hamstring exercise was done by straight leg lifting using a band three times for 15 seconds .

PROCEDURE

Infrared Group

Infrared Group received 20 minutes infrared to hamstring muscles region at prone position and participants stretchted the hamstring muscles at supine position.Self stretching hamstring exercise was done by straight leg lifting using a band three times for 15. seconds .

PROCEDURE

Ultrasound Group

Ultrasound Group received 5 minutes 1 M-Hz, 1,5 watt/cm2 ultrasound therapy to hamstring muscles region at prone position and participants stretched the hamstring muscles at supine position.Self stretching hamstring exercise was done by straight leg lifting using a band three times for 15 seconds .

PROCEDURE

Control

Control Group participants stretched the hamstring muscles at supine position.Self stretching hamstring exercise was done by straight leg lifting using a band three times for 15 seconds .

Sponsors & Collaborators

  • Pamukkale University

    lead OTHER

Principal Investigators

  • Atiye KAŞ ÖZDEMİR, Msc · Sarayköy Vocational School Turan Mah. Jeotermal Sok. No:1 Sarayköy, Denizli

  • Ummuhan BAŞ ASLAN, Prof .Dr. · Pamukkale Univercity 20070 Kınıklı Denizli, Turkey

  • Merve Bergin KORKMAZ, DR. · Denizli State Hospital 20040 Denizli, Turkey

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
25 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-04-22
Primary Completion
2020-04-25
Completion
2021-08-28

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04328155 on ClinicalTrials.gov