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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05582733
Other study ID # REC:00570
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 1, 2019
Est. completion date January 28, 2020

Study information

Verified date October 2022
Source University of Lahore
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To determine the immediate effects of cervical spine manipulation on pressure pain sensitivity on upper trapezius trigger point. it was a randomized control trial including 66 patients at physiotherapy OPD of railway rehabilitation center from August 2019 to December 2019, Railway General Hospital Pakistan and Max Rehab and decompression center Max health Hospital G8 Islamabad. The subjects were randomly divided into two groups (group control and experimental) by free envelope method.


Description:

To determine the immediate effects of cervical spine manipulation on pressure pain sensitivity on upper trapezius trigger point and neck ranges of motion. A randomized control trial of 66 patients was conducted from August 2019 to December 2019 at physiotherapy OPD of railway rehabilitation center, Railway General Hospital Pakistan and Max Rehab and decompression center Maxhealth Hospital G8 Islamabad. The subjects were randomly divided into two groups (group control and experimental) by free envelope method. Control was treated with Manual Pressure release followed by stretching while in experimental received cervical spine manipulation (chin hold) kaltenborn followed by stretching. Structural questionnaire was used for pre and post assessment. Outcomes were measured by algometry and inclinometer before and after the application of respective techniques. The data was analyzed at baseline and immediately after the intervention on IBM SPSS-21.


Recruitment information / eligibility

Status Completed
Enrollment 66
Est. completion date January 28, 2020
Est. primary completion date December 30, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 25 Years to 45 Years
Eligibility Inclusion Criteria: - 1.presence MTrps in upper trapezius - limited side bending and rotation - both gender - age between 25 to 45 Exclusion Criteria: - Malignancy, infection, trauma, bone deformities. - Acute Disc Protrusion - Positive VBI - Positive Sharp purser test - History of whiplash injury

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Cervical spine manipulation
hot pack for 10 minutes will be applied followed by cervical manipulation (chin hold kaltenborn) once and then stretching
traction
Hot pack will be applied followed by sustained pressure or MPR for 90 sec and then stretching.

Locations

Country Name City State
Pakistan Dr. Abdul Gaffoor Islamabad

Sponsors (2)

Lead Sponsor Collaborator
University of Lahore Riphah International University

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary changes from the baseline in Algometer values It is a device used to identify the pressure and force eliciting a pressure pain threshold. The hand held algometer 1 cm round rubber surface which applies force and display for readings in newtons or kilograms.Sustained force is usually applied at the right angle to the soft tissue. Estimated pressure application rates have ranged from 0.05 to 20N/s. it has a high validity and reliability for measuring pain pressure threshold in patients of myofascial trigger points. Baseline and 3 weeks
Primary changes from the baseline in Inclinometer values It is a device used to measure neck ranges of motion. Baseline and 3 weeks
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