- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06098053
Efficacy of Muscle Energy Technique Alone and in Combination With Interferential Therapy for the Treatment of Non-specific Low Back Pain.
October 18, 2023 updated by: Neuro Counsel Hospital, Pakistan
Single blind randomized control trail in which two groups were formed.
Group A was given Muscle energy technique and Group B was given muscle energy technique in combination with Interferential therapy.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
After getting the REC approval from The Neurocounsel Clinics, study was initiated from 21 May, 2023 to 20 September 2023.
Sample size was calculated by Epitool which came 30.
Following participants were included a) both genders b) age 20-50 years and followings were excluded a) DM b) Parkinson disease c) disc disorder d) MSK disorder were excluded from this study.
Simple random sampling technique was used to randomize participants into two equal groups.
group A was given MET and group B was given MET plus IFT. 2 sessions/week for 4 & half weeks.
Evaluation was done at PNS & EQ-5D-5L (QoL).
Pre and post test analysis was done by use of SPSS version 21 and level of significance was kept p<0.05.
Study Type
Interventional
Enrollment (Actual)
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 Locations
-
-
Federal
-
Islamabad, Federal, Pakistan, 44010
- The Neurocouncil Clinic
-
-
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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- both genders
- age between 20-50 years old
- non specific type of back pain
Exclusion Criteria:
- Diabetes Mellitus
- Parkinson disease
- Any other Musculoskeletal disorder
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: Group A
Muscle energy technique was given to this group
|
Muscle energy technique is used at a rate of three sessions per week for four and half weeks
|
|
Active Comparator: Group B
Muscle energy technique along with interferential therapy was given to this group
|
Muscle energy technique along with interferential therapy is used at a rate of three sessions per week for four and half weeks
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain numeric scale
Time Frame: 4 and half weeks
|
this scale is used to measure the pain 0 means no pain and 10 means worst pain ever
|
4 and half weeks
|
|
short form of 36
Time Frame: 4 and half weeks
|
SF-36 is used to meaure the quality of life.
0 means worst quality of life and higher values towards 100 means best quality of life
|
4 and half weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
May 21, 2023
Primary Completion (Actual)
September 20, 2023
Study Completion (Actual)
September 20, 2023
Study Registration Dates
First Submitted
October 18, 2023
First Submitted That Met QC Criteria
October 18, 2023
First Posted (Actual)
October 24, 2023
Study Record Updates
Last Update Posted (Actual)
October 24, 2023
Last Update Submitted That Met QC Criteria
October 18, 2023
Last Verified
October 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 348
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
have not decided anything yet
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.
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