Comparative Effect of ART and MET on Pain, ROM and Functional Disability in AC Patients With Trigger Points

Adhesive Capsulitis Clinical Trial

Official title:

Comparative Effect of Active Release Technique and Muscles Energy Technique on Pain, ROM and Functional Disability in Adhesive Capsulitis Patients With Trigger Points

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT05448612
• Other study ID #: REC-UOL-/98-04/2022
• Status: Active, not recruiting
• Phase: N/A
• Start date: January 10, 2022
• Est. completion date: September 30, 2022

Study information

• Verified date: May 2022
• Source: University of Lahore
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The aim of this study to determine the Comparative effect of active release technique and muscle energy technique on pain, ROM and functional disability in adhesive capsulitis patients with trigger points.

Description:

74 participants are included in this study in two groups and 37 for each group. Group A for active release technique along with conventional therapy and Group B for muscles energy technique along with conventional therapy.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 74
• Est. completion date: September 30, 2022
• Est. primary completion date: February 25, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 40 Years to 60 Years

Eligibility

Inclusion Criteria:

• Both male and female.

• Participants having unilateral adhesive capsulitis.

• Participants with sub-acute adhesive capsulitis.

• Participants having age of 40-60 years.

Exclusion Criteria:

• Patient with cervical radiculopathy.

• Fractures of upper limb.

• Thoracic outlet syndrome.

• Post-traumatic.

Related Conditions & MeSH terms

• Adhesive Capsulitis
• Bursitis

Intervention

Other:
• Active Release Technique and muscle energy technique
74 participants divided into two groups and 37 in each group.

Locations

Country	Name	City	State
Pakistan	Spot Rehab	Lahore

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	patients rate their pain from 0 to 10, from 0 to 20, or from 0 to 100. Zero represents "no pain," whereas 10, 20, or 100 represents the opposite end of the pain continuum (e.g., "the most intense pain imaginable," "pain as intense as it could be," "maximum pain").	Change from Baseline in pain to 6 week
Primary	Universal Goniometry	Universal goniometer (UG) is commonly used as a standard method to evaluate range of motion (ROM) as part of joint motions.	Change from Baseline in range of motion to 6 week
Primary	Shoulder Pain and Functional Disability Index	The Shoulder Pain and Disability Index (SPADI) is a self-administered questionnaire consisting of items grouped into pain and disability subscales.	Change from Baseline in disability to 6 week