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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04244045
Other study ID # P.T.REC/012/002566
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2019
Est. completion date December 30, 2019

Study information

Verified date January 2020
Source Jouf University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

45 female participants with short hamstring syndrome were devided into one of the three groups; Group I: suboccipital muscle inhinbition plus passive hamstring stretch, group II: Slump stretch position plus Passive hamstring stretch, and group III: Passive stretch of hamstring muscle. Assessment methods were Straight leg raising test, forward flexion test and popliteal angle test, were measured at baseline, immediately after 1st treatment session then after 4 weeks of treatment.


Description:

Forty five university undergraduate female students volunteered to participate in the study, age = 18-25 years old, body mass index 18-25 kg/cm square.

All subjects were free from injury or disease expected to affect hamstring length or ability to perform the exercises Design of the study was single-blind randomized clinical trial. The subjects were randomly assigned in to one of the three methods of treatment, which are group 1 (study group1): suboccipital muscle inhibition plus passive stretch of hamstring muscle, Group II: ( Study groupII): received neural slump test position plus passive stretch of hamstring muscle, Group III (control group): received only passive stretch of hamstring muscle.

Treatment Procedures:

Passive stretching of hamstring muscle:

Patient in comfortable supine lying position and therapist stride standing beside the dominant side of the patient. The patient was asked to flex his hip joint with complete knee extension and ankle in neutral position. The therapist stretches the hamstring of the dominant side; distal hand of the therapist on planter surface of foot for dorsiflexion to increase flexibility of hamstring muscle and proximal hand on the knee to increase the length of the muscle, maintain this stretching for 60 seconds then relax (8)

Sub occipital muscle inhibition:

The Patient is in comfortable supine lying position with eye closed - for more relaxation- and the head out of the bed resting on therapist hand to manipulate the sub occipital area. The therapist stretch the sub occipital, flexes the head of the patient to get the chin to the manibiurim sternii, maintaining this position for 60seconds then relax (9)

Neural dynamic slump stretch:

Patient in comfortable short sitting position at the edge of the bed with the trunk in an millitary straight position then ask the patient to slump the flex his neck and street the knee joint in complete extension the at the end of the procedure do active dorsiflexion at the tested foot .(10)


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date December 30, 2019
Est. primary completion date December 30, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 28 Years
Eligibility Inclusion Criteria:

1. Being females.

2. Age between 18-28 years old.

3. BMI: 18-25 kg/square meter.

4. All subjects were free from injury or disease expected to affect hamstring length or ability to perform the exercises.

5. Straight leg raising test (SLR) is less than 80 degree from supine position.

6. Popliteal angle test, operationally defined by a knee flexion angle greater than 15° as measured by a screening exam using active knee extension in supine with hip flexed 90°

Exclusion Criteria:

- Hamstring injury within the past year.

- Exceeding 80° in the initial SLR test. Popleteal knee angle less than 15 degree. -

- Verbal report of performing regular lower extremity. Muscle stretching exercises.

- History of neck trauma (whiplash). Neck symptoms.-

- History of recent fracture in any part of the body.

- History of growth disorders,

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Suboccipital muscle inhibition
The patient was asked to flex his hip joint with complete knee extension and ankle in neutral position. The therapist stretches the hamstring of the dominant side; distal hand of the therapist on planter surface of foot for dorsiflexion. and proximal hand on the knee to increase the length of the muscle, maintain this stretching for 60 seconds then relax .Sub occipital muscle inhibition: The Patient is supine, The therapist stretch the sub occipital, flexes the head of the patient to get the chin to the manibiurim sternii, maintaining this position for 60seconds then relax Slump strtch position:Patient in comfortable short sitting position at the edge of the bed with the trunk in an millitary straight position then ask the patient to slump the flex his neck and street the knee joint in complete extension the at the end of the procedure do active dorsiflexion at the tested foot

Locations

Country Name City State
Egypt Faculty of physical therapy, Cairo University. Cairo

Sponsors (5)

Lead Sponsor Collaborator
Jouf University Alaa Mohamed Al abbas, Cairo University, Olfat Ibrahim Ali, Sara Hamed Elzarea

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Straight leg raising test the patient was supine lying position with hip and knee extension at the starting position, then the patient was asked to actively flex hip joint as much as possible while maintaining the knee in extension position. Then with the goniometer the therapist started to determine the angle of hip flexion, patients were excluded if the SRL was more than 80°at the initial evaluation after 4 weeks of intervention.
Secondary Popliteal Angle Test while the patient was in supine line position, the hip and knee joint was flexed to 90° then the patient was asked to extend the knee joint as much as possible with maintaining the hip in flexion 90°. Then with the goniometer the therapist determines the angle of the knee flexion, subjects were excluded if their angle of flexion less than 15 ° after 4 weeks of intervention.
Secondary Forward flexion test the patient was stride standing on footstep facing the therapist and then asked to flex her trunk with his hands facing forward, maintaining the knee in extended position. The therapist then measures the distance between the middle finger and the ground while the trunk is in complete flexion. after 4 weeks of treatment.
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