NCT04932707

Brief Summary

The hamstrings muscles are examples of muscle groups that have a tendency to shorten. Limited flexibility has been shown to predispose a person to several musculoskeletal overuse injuries and significantly affect a person's function.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
117

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jul 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 12, 2021

Completed
9 days until next milestone

First Posted

Study publicly available on registry

June 21, 2021

Completed
2.1 years until next milestone

Study Start

First participant enrolled

July 16, 2023

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 15, 2024

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

March 28, 2024

Completed
Last Updated

July 23, 2024

Status Verified

July 1, 2024

Enrollment Period

7 months

First QC Date

June 12, 2021

Last Update Submit

July 21, 2024

Conditions

Keywords

hamstringStretchSub-occipital inhibitionNeuro-dynamic

Outcome Measures

Primary Outcomes (2)

  • knee extension angle test

    Measure the knee extension knee joint from a supine lying position with hip and knee joints flexed to 90 degree.

    Immediately after the procedure

  • knee extension angle test

    Measure the knee extension knee joint from a supine lying position with hip and knee joints flexed to 90 degree.

    4 weeks

Secondary Outcomes (4)

  • Straight leg raising test

    Immediately after the procedure

  • Straight leg raising test

    4 weeks

  • Forward flexion test

    Immediately after the procedure

  • Forward flexion test

    4 weeks

Study Arms (3)

Study group 1

EXPERIMENTAL

sub-occipital muscle inhibition.

Other: sub-occipital muscle inhibition techniqueOther: control (passive stretch exercises)

Study group 2

EXPERIMENTAL

Received neurodynamic mobilization.

Other: Neurodynamic mobilizationOther: control (passive stretch exercises)

control group

ACTIVE COMPARATOR

Received passive stretch of the hamstring muscle.

Other: control (passive stretch exercises)

Interventions

this technique will be conducted from a supine lying position. The therapist stretches the suboccipital, placing the hands beneath the patient's head applying pressure up and backward, pressure was maintained till tissue relaxation occurred flexes the head of the patient to get the chin to the manibiurim sternm.

Study group 1

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

Study group 2

The patient in a comfortable supine lying position, 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

Study group 1Study group 2control group

Eligibility Criteria

Age18 Years - 25 Years
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • undergraduate female students
  • body mass index 18-25 kg/cm square.
  • All subjects will be free from injury or disease expected to affect hamstring length or ability to perform the exercises.

You may not qualify if:

  • Hamstring injury within the past year.
  • Verbal report of performing regular lower extremity.
  • Current Muscle stretching exercises.
  • History of neck trauma (whiplash).
  • History of recent fracture in any part of the body.
  • History of neurological or orthopedic disorders
  • Diagnosis of a herniated disk
  • Low back pain in the last 6 months

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Olfat Ibrahim Ali

Giza, Dokki, 12611, Egypt

Location

Study Officials

  • Olfat I Ali, PhD

    Cairo University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

June 12, 2021

First Posted

June 21, 2021

Study Start

July 16, 2023

Primary Completion

February 15, 2024

Study Completion

March 28, 2024

Last Updated

July 23, 2024

Record last verified: 2024-07

Data Sharing

IPD Sharing
Will share

Sharing will be possible after the publication of the study

Shared Documents
STUDY PROTOCOL
Time Frame
After study publication
Access Criteria
Contact: Olfat Ibrahim Ali, email address: olfat\ ib@yahoo.com, olfat\ ib@cu.edu.eg

Locations