- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05058820
Post Facilitation Stretch Versus Active Isolated Stretching Along With Deep Friction Massage in Wallet Sciatica.
October 19, 2021 updated by: Riphah International University
Effects of Post Facilitation Stretch Versus Active Isolated Stretching Along With Deep Friction Massage in Wallet Sciatica.
To compare the effects of post facilitation stretch and active isolated stretch along with deep friction massage on pain pressure threshold of trigger points, disability, muscle length, and hip joint range of motion in wallet sciatica.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Literature shows the effectiveness of both techniques post facilitation stretch and active isolated stretch but didn't report any comparison.
In this study, investigator diagnosed the patients with wallet sciatica who came with the complaint of low back pain.
Both techniques were compared to determine the effectiveness in patients with wallet sciatica having trigger points.
Study Type
Interventional
Enrollment (Anticipated)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Momena Shahzad, MSPT-OMPT
- Phone Number: +92-334-2848148
- Email: momena.shahzad@riphah.edu.pk
Study Locations
-
-
Fedral
-
Islamabad, Fedral, Pakistan, 44000
- Recruiting
- Ali Ahmad Physio Care, F-7/2
-
Contact:
- Momena Shahzad, MS-OMPT
- Phone Number: +92-334-2848148
- Email: momena.shahzad@riphah.edu.pk
-
Principal Investigator:
- Samira Sabir, MS-OMPT*
-
-
Punjab
-
Rawalpindi, Punjab, Pakistan, 46000
- Recruiting
- Railway General Hospital
-
Contact:
- Momena Shahzad, MS-OMPT
- Phone Number: +92-334-2848148
- Email: momena.shahzad@riphah.edu.pk
-
Principal Investigator:
- Samira Sabir, MS-OMPT*
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
25 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Pain (Grade greater than 3)
- Chronic pain (greater than 3 months) buttock pain.
- Patients with piriformis tightness less than 40 degrees.
- Patients with active trigger points of the piriformis.
Exclusion Criteria:
- Patient with tumor
- Patients with cognitive problems.
- Recent or history of hip trauma or injury.
- Recent abdominal surgery.
- Any other orthopedic or neurological condition of hip and lumbar spine
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Post Facilitation stretch
Hot pack, TENS, Post Facilitation stretch, Deep friction massage
|
Hot pack 10 mins/ 1set/ (3 days/ week), TENS 10 mins/ 1 set/ (3 days/ week), Post facilitation stretch 15 secs isometric hold/ 15 secs stretch/ 30 secs relax/ 5 reps/ 1 set/ (3 days/ week), Deep friction massage 5 minutes/ (3 days/ week).
A total of 6 weeks (18 sessions, 3 days/ week) were given each consisting of 30 mins.
|
|
Active Comparator: Active Isolated Stretching
Hot pack, TENS, Active Isolated Stretching, Deep friction massage
|
Hot pack 10 mins/ 1set/ (3 days/ week), TENS 10 mins/ 1 set/ (3 days/ week), Active Isolated Stretching 2 secs hold/ 10 reps/ 1 set/ (3 days/ week), Deep friction massage 5 minutes/ (3 days/ week).
A total of 6 weeks (18 sessions, 3 days/ week) were given each consisting of 30 mins.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain pressure threshold
Time Frame: 18 days
|
Changes from baseline, Pain pressure threshold was measured through Algometer.
|
18 days
|
|
Disability
Time Frame: 18 days
|
Changes from baseline, Disability was measured through lower extremity functional scale.
It consists of 20 questions.
Minimum score is 0 and Maximum 80. minimum score shows greater disability and maximum indicate decreased disability.
|
18 days
|
|
Piriformis Muscle Length
Time Frame: 18 days
|
Changes from baseline, Piriformis Muscle Length was measured through Goniometer by performing stretch test.
Less than 40 degree internal rotation at hip indicates piriformis tightness.
|
18 days
|
|
Hip joint range of motion
Time Frame: 18 days
|
Changes from baseline, Hip joint range of motion was measured through Goniometer.
|
18 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Momena Shahzad, MS-OMPT, Riphah International University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 3, 2021
Primary Completion (Anticipated)
December 15, 2021
Study Completion (Anticipated)
February 28, 2022
Study Registration Dates
First Submitted
September 17, 2021
First Submitted That Met QC Criteria
September 17, 2021
First Posted (Actual)
September 28, 2021
Study Record Updates
Last Update Posted (Actual)
October 21, 2021
Last Update Submitted That Met QC Criteria
October 19, 2021
Last Verified
October 1, 2021
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/0971 Samira Sabir
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Wallet Sciatica
-
Kaiser PermanenteCompletedSciatica Pain | Sciatica AcuteUnited States
-
Riphah International UniversityRecruitingSciatica | Sciatica PainPakistan
-
Prince Sattam Bin Abdulaziz UniversityCompleted
-
Istinye UniversityRecruitingSciatica Pain | Sciatica Acute | Mulligan MobilizationTurkey (Türkiye)
-
Primus PharmaceuticalsIllumination HealthRecruitingLumbar Spinal Stenosis | Sciatica AcuteUnited States
-
University of LahoreRecruitingPain | Acute SciaticaPakistan
-
Pakistan Institute of Medical SciencesRiphah International UniversityCompletedSciatica | Sciatica AcutePakistan
-
St George Hospital, AustraliaSt George & Sutherland Medical Research FoundationUnknown
-
University Hospital, MontpellierUnknown
-
Nantes University HospitalTerminatedDiscal SciaticaFrance
Clinical Trials on Post Facilitation stretch
-
Riphah International UniversityRecruitingAutism Spectrum DisorderPakistan
-
Riphah International UniversityCompleted
-
Riphah International UniversityCompletedDisability | Range of Motion | Flexibility | HamstringsPakistan
-
Riphah International UniversityCompletedPost Traumatic Stiff ElbowPakistan
-
Riphah International UniversityCompleted
-
Foundation University IslamabadRecruiting
-
Ibadat International University, IslamabadCompleted
-
Neuro Counsel Hospital, PakistanAl Nafees Medical Hospital, Islamabad; National Institute of Rehabilitation...CompletedShoulder Impingement SyndromePakistan
-
Foundation University IslamabadRecruitingQuadratus Lumborum SyndromePakistan
-
Cairo UniversityRecruiting