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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05686811
Other study ID # REC-UOL-/226-09/2022
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 26, 2021
Est. completion date July 28, 2022

Study information

Verified date January 2023
Source University of Lahore
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

COMPARATIVE EFFECTS OF MYOFASCIAL RELEASE THERAPY AND POST ISOMETRIC RELAXATION TECHNIQUE ON PAIN AND FUNCTIONAL DISABILITY IN PATIENTS WITH TENSION-TYPE HEADACHE


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.


Recruitment information / eligibility

Status Completed
Enrollment 72
Est. completion date July 28, 2022
Est. primary completion date July 28, 2022
Accepts healthy volunteers No
Gender All
Age group 20 Years to 45 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Other:
Myofascial release therapy therapy
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
Post isometric relaxation technique
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.

Locations

Country Name City State
Pakistan Abdul Mateen Lahore Punjab

Sponsors (1)

Lead Sponsor Collaborator
University of Lahore

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Numerical pain rating scale 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
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