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Optimal Duration of Stretching of the Hamstring Muscle Group in Elderly: A Randomized Controlled Trial

Optimal Time of Hamstring Stretch in Elderly

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04459832
Enrollment
105
Registered
2020-07-07
Start date
2020-07-31
Completion date
2020-08-31
Last updated
2020-07-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stretch

Keywords

Stretching, Randomized controlled trial, Hamstring

Brief summary

identification of optimal duration for hamstring muscle stretch by using 3 different time of stretch 15,30,60 seconds .100 subjects will be participated in this study divided into 4 group one control and 3 experimental groups according to stretch time.

Detailed description

Abstract: OBJECTIVE: To explore the effect of variable stretching intervals on neural function and ROM. DESIGN: Randomized controlled trial Participants: In this trial, 100 participants will participate in the study diagnosed with tight hamstring muscles (defined as the inability to extend the knee to less than 20° of knee flexion) were randomly assigned to the control group or one of the 3 intervention groups Interventions: The three experimental groups will stretched 5 times per week for 4 weeks for 15, 30, and 60 seconds, respectively the control group did not stretch Main Outcome Measures: The neurophysiological outcome measures included peak to peak somatosensory evoked potential for dermatomes L3,L4,L5, and S1. Secondary outcome measures included knee ROM. All outcome measures will be assessed immediately after the treatment session and 24 hours after the treatment session.

Interventions

PROCEDUREstretch hamstring

Stretching of the hamstring muscles was performed by the primary researcher. A straight-leg-raising technique was used for this stretch because we believe that it is commonly used in the clinical setting for elderly people. All subjects were supine lying as flat as possible

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

The assessor, who took the measurements for both the intervention and control groups, was blinded to the subject's group, while the treating therapist was not blinded to the treatment intervention.

Intervention model description

randomized controlled trial study 100 participants will be recruited to participate in the study after assigning a conset form, participants will be divided into 4 group ,one control which will not receive stretch of hamstring and 3 experimental groups will recive different duration for hamstring stretch 15,30,60 and DSSEP will be measured as the primary outcome and knee ROM will be measured as a secondary outcomes in order to identify the optimal duration of hamstring stretch

Eligibility

Sex/Gender
ALL
Age
55 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Subjects had to demonstrate tight hamstring muscles, defined as inability to extend the knee to less than 20 degrees of knee flexion with the femur held at 90 degrees of hip flexion while the person was positioned supine. Subjects were also screened to rule out knee joint flexion contractures by checking knee extension ROM, while they were lying in a prone position

Exclusion criteria

* Using of medical aids, and suffering from any neurological or cognitive impairment, limiting cardio-respiratory conditions, or had undergone recent surgery (within the past 12 months). Having any hip or knee replacements or any history of pathology in the low back, hips, or knees for the 3 months prior to the study

Design outcomes

Primary

MeasureTime frameDescription
Neurophysiological findings.Assessments of the change of DSSEPs from baseline to immediatly after session and at 24 hour after sessionNeurophysiological findings included peak to peak somatosensory evoked potentials (DSSEPs) for L3,L4,L5,S1 dermatomes.

Secondary

MeasureTime frameDescription
ROMAssessments of the change of Knee ROM from baseline to immediatly after session and at 24 hour after sessionEach subject was then measured for knee extension ROM on both lower extremities

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026