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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05059496
Other study ID # REC/00854 Maryum Rahim
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date October 13, 2020
Est. completion date February 28, 2022

Study information

Verified date September 2021
Source Riphah International University
Contact Momena Shahzad, MS
Phone +92-334-2848148
Email momena.shahzad@riphah.edu.pk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To determine the effects of Hamstring stretching using a pressure Biofeedback unit on muscle length, pain, and functional status in patients with low back pain.


Description:

Several studies have been conducted regarding hamstring stretching with the pelvis anteriorly tilted for treating low back pain but there is very little evidence regarding the use of a pressure biofeedback unit for maintaining anterior pelvic tilt so this study aims to find out whether the hamstring stretching while maintaining anterior pelvic tilt using pressure biofeedback is more effective than hamstring stretching without using pressure biofeedback in patients with low back pain.


Recruitment information / eligibility

Status Recruiting
Enrollment 38
Est. completion date February 28, 2022
Est. primary completion date September 30, 2021
Accepts healthy volunteers No
Gender All
Age group 25 Years to 40 Years
Eligibility Inclusion Criteria: - Patients with non-specific low back pain - Chronic pain > 3 months - Participants having (ODI) score minimum 20% to 40% - Participants with hamstrings shorter than 70 degrees bilaterally - Participants who scored 3 or more than 3 on the Numeric Pain Rating Scale (NPRS) Exclusion Criteria: - History of fracture and surgery - Patients with osteoarthritis and spondylolisthesis - Patients with systemic disease except for diabetes mellitus and hypertension - Patients with disc herniation and leg length discrepancy - Pregnant females - Participants with severe back pain or excessive lumber lordosis

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Hamstring stretching with Pressure Biofeedback Unit
Hot Pack 15 mins/1 set/ (3 days/week), Hamstring stretching with Pressure Biofeedback Unit 30 secs hold/ 15 secs rest/ 3 sets/ (3 days/week), TENS 15 mins/ 1 set/ (3 days/week). A total of 4 weeks (12 sessions, 3 days/ week) were given each consisting of 35 mins.
Hamstring stretching with out Pressure Biofeedback Unit
Hot Pack 15 mins/1 set/ (3 days/week), Hamstring stretching without Pressure Biofeedback Unit 30 secs hold/ 15 secs rest/ 3 sets/ (3 days/week), TENS 15 mins/ 1 set/ (3 days/week). A total of 4 weeks (12 sessions, 3 days/ week) were given each consisting of 35 mins.

Locations

Country Name City State
Pakistan Railway General Hospital Rawalpindi Punjab

Sponsors (1)

Lead Sponsor Collaborator
Riphah International University

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Hamstring Length Changes from baseline, Hamstring length was measured through Goniometer. Normal value of Active knee extension is 90 degree with 90 degree hip flexion. Values less than 70 degree knee extension represents hamstring tightness. 12 days
Secondary Pain through NPRS Changes from baseline, Pain was measured through Numeric pain rating scale. 0 represents "no pain" and 10 "worst pain possible". 12 days
Secondary Functional Status Changes from baseline, Functional status was measured through Oswestry Disability Index. 0-20 shows "minimal disability", 21-40 "moderate disability", 41-60 "severe disability", 61-80 "crippled" and 81-100 "bed bound patients". 12 days
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