Effectiveness of Kaltenborn End Range Joint Mobilization Technique and Post FacilitationStretch in Shoulder Impingement Syndrome

NCT05871944 | Completed DMC

• 1 other identifier: 341
• Study Type: interventional
• Target: 20
• Locations: 1 country
• Sites: 1

Brief Summary

This study is a experimental one to observe the efficacy of joint mobilization and post facilitation techniques in shoulder impingement syndrome

Conditions

Shoulder Impingement Syndrome

Outcome Measures

Primary Outcomes (2)

• Goniometer

  This is a instrument designed to evaluate the joint range of motion. Greater ranges mean more mobility of joint and less means more restriction

  4 weeks

• Shoulder Pain and Disability Index

  Used to assess the patients level of pain and the ADLs which are affected. O score means no dysfuction of joint and higer score means more dysfuction

  4 weeks

Study Arms (2)

control group

ACTIVE COMPARATOR

kalternborn joint mobilization techniques will be administered for total of 8 weeks at the rate of 2 session per week.

Other: KAlternborn Joint Mobilization

experimental group

EXPERIMENTAL

Post stretch facilitation technique will be administered for total of 8 weeks at the rate of 2 session per week.

Other: Post stretch Facilitation Technique

Interventions

KAlternborn Joint Mobilization OTHER

This is a join mobilization technique to reduce the joint stiffness and help in improving joint range of motion

control group

Post stretch Facilitation Technique OTHER

This is a PNF techniques used to relax the muscles and help in getting more free range of restricted joint

experimental group

Eligibility Criteria

• Age: 25 Years - 45 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Both male and female
• Age 25 to 45
• Diagnosed Rotator cuff impingement from ortho, neuro and musculoskeletal department
• Hawkin kennedy test positive
• Neer's test positive
• Jobe's test positive

You may not qualify if:

• Cervical spine disorder
• Fractures
• Major upper limb surgery
• Tumor or wound
• Diagnosed acromial malformations

Sponsors & Collaborators

• Neuro Counsel Hospital, Pakistan: lead
• Al Nafees Medical Hospital, Islamabad: collaborator
• National Institute of Rehabilitation Medicine, Islamabad, Pakistan: collaborator

Study Sites (1)

Al Nafees Medical Hospital, Islamabd

Islamabad, Federal, 44000, Pakistan

Location

MeSH Terms

Conditions

Shoulder Impingement Syndrome

Condition Hierarchy (Ancestors)

Joint Diseases; Musculoskeletal Diseases; Shoulder Injuries; Wounds and Injuries

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: PARTICIPANT
• Masking Details: This will be single blind randomized control clinical trail in which just participant will be unware about which group he/she is included
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Model Details: Two groups will be formed. one group will receive joint mobilization technique and other will get post facilitation stretch technique

Study Record Dates

• First Submitted: May 13, 2023
• First Posted: May 23, 2023
• Study Start: January 5, 2023
• Primary Completion: May 4, 2023
• Study Completion: May 4, 2023
• Last Updated: May 23, 2023

Record last verified: 2023-05

Locations

PA (1)