- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05686811
Tension Type Headache, Myofascial Release Therapy , Post Isometric Relaxation Technique
January 13, 2023 updated by: University of Lahore
Comparative Effect of Myofascial Release Therapy and Post Isometric Relaxation Technique on Pain and Functional Disability in Patients With Tension Type Headache
COMPARATIVE EFFECTS OF MYOFASCIAL RELEASE THERAPY AND POST ISOMETRIC RELAXATION TECHNIQUE ON PAIN AND FUNCTIONAL DISABILITY IN PATIENTS WITH TENSION-TYPE HEADACHE
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Tension-type headache (TTH) is the most common type of primary headache, typically presenting as a bilateral, non-throbbing headache with mild to moderate intensity.
Patients with tension-type headache often report band-like tightness and increased tenderness of the pericranial muscles.
Use of myofascial release technique and post isometric relaxation technique is believed to reduce the pain and improve the functional disability.
Study Type
Interventional
Enrollment (Actual)
72
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
-
-
Punjab
-
Lahore, Punjab, Pakistan, 54000
- Abdul Mateen
-
-
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
20 years to 45 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
• Age range 25-45years14
- Both male and females
- Suffer from tension type headache more than three months
- Head pain on bilateral location
- may suffer from photophobia, phonophobia
- Pericranial tiredness
- not getting enough exercise or sleep
Exclusion Criteria:
• History of teeth clenching or grinding
- Cardiovascular disease
- Pregnancy
- arthritis in the neck
- being overweight
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: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Myofascial release therapy
This group will receive routine physical therapy with myofascial release therapy.This protocol will be given for 3 alternative days per week.
Each session will be of 40 minutes.
Data will be calculated at baseline , at 2nd and at 4th week.
|
Group A was treated with myofascial release therapy and routine physical therapy.
For routine physical therapy subjects will first applied TENS, hot pack and neck isometric exercises then myofascial release therapy will be given.
For myofascial release therapy subjects was in the supine or possibly sitting position, the examiner was seated at the head of the table, the examiner was used his right thumb to palpate (using flat palpation) the upper trapezius muscles from medial to lateral to establish if any MTrPs are present.
The entire mass of the upper trapezius muscle is lifted by the supraspinatus muscle and grasped with a pincer grasp.
The muscles at this point rotate between the thumb and forefinger to detect the delicate location of the trigger point.
Treatment session longs for 10 minutes of myofascial release on each side
|
Experimental: post isometric relaxation technique
This group will receive routine physical therapy with post isometric relaxation technique.This protocol will be given for 3 alternative days per week.
Each session will be of 40 minutes.
Data will be calculated at baseline , at 2nd and at 4th week.
|
This group will receive routine physical therapy with myofascial release therapy.This protocol will be given for 3 alternative days per week.
Each session will be of 40 minutes.
Data will be calculated at baseline , at 2nd and at 4th week.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Numerical pain rating scale
Time Frame: at the end of 4th week
|
The Numerical Pain Rating Scale (NPRS) is a subjective measure in which individuals rate their pain on an eleven-point numerical scale.
The scale is composed of 0 (no pain at all) to 10 (worst imaginable pain).
|
at the end of 4th week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Abdul Mateen, MS(msk), University of Lahore
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)
October 26, 2021
Primary Completion (Actual)
July 28, 2022
Study Completion (Actual)
July 28, 2022
Study Registration Dates
First Submitted
October 24, 2022
First Submitted That Met QC Criteria
January 13, 2023
First Posted (Estimate)
January 16, 2023
Study Record Updates
Last Update Posted (Estimate)
January 16, 2023
Last Update Submitted That Met QC Criteria
January 13, 2023
Last Verified
January 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC-UOL-/226-09/2022
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 Neck Pain
-
Fatih TekinPamukkale UniversityCompletedChronic Neck Pain | Persistent Neck Pain | Neuroscience ApproachTurkey
-
Hacettepe UniversityRecruitingNeck Pain | Cervical Pain | Neck Pain, Posterior | Neck Muscle Issue | Cervical Pain, PosteriorTurkey
-
Jeff Elias, MDRecruitingCancer of Head and Neck | Pain, Neck | Pain, FaceUnited States
-
Riphah International UniversityCompleted
-
Instituto Brasileiro de OsteopatiaCompletedNeck Pain | Pain, NeckBrazil
-
Riphah International UniversityCompletedCervical Pain | Mechanical Neck PainPakistan
-
Ankara UniversityCompleted
-
Josue Fernandez CarneroCentro Universitario La SalleCompleted
-
Sakarya UniversityUnknown
-
Shanghai University of Traditional Chinese MedicineBeijing Hospital; Dongzhimen Hospital, Beijing; Traditional Chinese Medicine... and other collaboratorsNot yet recruiting
Clinical Trials on Myofascial release therapy therapy
-
Marmara UniversityCompletedSports Physical Therapy | Basketball Players | Myofascial Release Technique | Performance EnhancementTurkey
-
Riphah International UniversityRecruiting
-
Universidad de la SabanaUnknownAnkylosing Spondylitis
-
Universidad de AlmeriaCompleted
-
Istanbul Medipol University HospitalCompleted
-
Zeng ChanghaoPeople's Hospital of Zhengzhou UniversityNot yet recruiting
-
Copka SonpashanNot yet recruiting
-
Copka SonpashanNot yet recruiting
-
Copka SonpashanNot yet recruitingTraumatic Brain Injury
-
Zeng ChanghaoRecruitingTraumatic Brain InjuryHong Kong