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

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

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

Study Overview

• Status: Completed
• Conditions: Shoulder Impingement Syndrome
• Intervention / Treatment: Other: KAlternborn Joint Mobilization; Other: Post stretch Facilitation Technique

Detailed Description

his study is a experimental one to observe the efficacy of Kalternborn end range joint mobilization and post facilitation techniques in shoulder impingement syndrome. Goniometer, shoulder disability index will be the tool used for evaluation

• Study Type: Interventional
• Enrollment (Actual): 20
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Pakistan
  • Federal
    • Islamabad, Federal, Pakistan, 44000
      • Al Nafees Medical Hospital, Islamabd

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

• 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

Exclusion Criteria:

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

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Single

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: control group; kalternborn joint mobilization techniques will be administered for total of 8 weeks at the rate of 2 session per week.	Other: KAlternborn Joint Mobilization; This is a join mobilization technique to reduce the joint stiffness and help in improving joint range of motion
Experimental: experimental group; 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; This is a PNF techniques used to relax the muscles and help in getting more free range of restricted joint

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
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

Collaborators and Investigators

• Sponsor: Neuro Counsel Hospital, Pakistan
• Collaborators: Al Nafees Medical Hospital, Islamabad; National Institute of Rehabilitation Medicine, Islamabad, Pakistan

Study record dates

Study Major Dates

• Study Start (Actual): January 5, 2023
• Primary Completion (Actual): May 4, 2023
• Study Completion (Actual): May 4, 2023

Study Registration Dates

• First Submitted: May 13, 2023
• First Submitted That Met QC Criteria: May 22, 2023
• First Posted (Actual): May 23, 2023

Study Record Updates

• Last Update Posted (Actual): May 23, 2023
• Last Update Submitted That Met QC Criteria: May 22, 2023
• Last Verified: May 1, 2023

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Pathologic Processes; Wounds and Injuries; Disease; Joint Diseases; Musculoskeletal Diseases; Rupture; Shoulder Injuries; Tendon Injuries; Syndrome; Rotator Cuff Injuries; Shoulder Impingement Syndrome
• Other Study ID Numbers: 341

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: UNDECIDED
• IPD Plan Description: Have not decided yet about this.

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No