Tele-rehabilitation With and Without Self-Mulligan Technique in Subacromial Pain Syndrome
TRIMS
Effects of Tele-rehabilitation With and Without Self-Mulligan Technique on Pain Range of Motion and Functional Disability in Subacromial Pain Syndrome
1 other identifier
interventional
52
1 country
1
Brief Summary
The present study demonstrated statistically significant improvements in pain, range of motion (ROM), and functional disability in both groups; however, participants receiving telerehabilitation with self-Mulligan technique exhibited significantly greater improvements compared to those receiving telerehabilitation alone. These findings highlight the added value of incorporating manual therapy concepts, even in a self- applied or remotely guided format, into rehabilitation programs for patients with subacromial pain syndrome (SAPS). The significant reduction in pain scores (VAS) and improvement in ROM across all planes in Group A can be explained by the biomechanical correction principle of the Mulligan Concept, particularly Mobilization with Movement (MWM). This technique is believed to correct minor positional faults in the glenohumeral joint, thereby restoring normal arthrokinematics, reducing nociceptive input, and improving movement efficiency. When combined with structured telerehabilitation exercises, it likely created a synergistic effect addressing both mechanical dysfunction and neuromuscular control.(25)
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 5, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 10, 2026
CompletedFirst Submitted
Initial submission to the registry
May 13, 2026
CompletedFirst Posted
Study publicly available on registry
May 28, 2026
CompletedMay 28, 2026
May 1, 2026
1.2 years
May 13, 2026
May 22, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Pain intensity
Pain was be measured using the Visual Analogue Scale (VAS) ranging from 0 (no pain) to 10 (worst pain). A mean reduction of ≥2 points after intervention was indicate a clinically significant improvement
Baseline and 6 weeks
Functional Disability
Functional limitation was assessed using SPADI(Shoulder pain and disability index). A post-treatment improvement of 8-13 points in SPADI(Shoulder pain and disability index) would represent meaningful functional recovery
Baseline and six weeks
Secondary Outcomes (1)
Range of motion
Baseline and 6 weeks post intervention
Study Arms (2)
Tele-rehabilitation without self mulligan technique
EXPERIMENTALParticipants will receive a structured tele-rehabilitation program for subacromial pain syndrome.
Tele-rehabilitation with self mulligan technique.
EXPERIMENTALParticipants will receive a structured tele-rehabilitation program with self Mulligan mobilization techniques.
Interventions
Participants will receive a structured tele-rehabilitation program combined with self-administered Mulligan mobilization with movement techniques for subacromial pain syndrome. Tele-rehabilitation will include supervised online physiotherapy sessions consisting of shoulder range of motion exercises strengthening exercises stretching postural correction and home exercise guidance delivered virtually. Self-Mulligan techniques will be taught and performed by participants under physiotherapist supervision.
Participants performed self Mulligan mobilization with movement techniques for the shoulder under physiotherapist supervision in addition to the tele-rehabilitation program. The intervention aimed to reduce pain and improve shoulder range of motion and functional disability in patients with subacromial pain syndrome.
Eligibility Criteria
You may qualify if:
- Individuals aged 25 to 55 years
- Clinically diagnosed with subacromial pain syndrome or subacromial impingement confirmed through orthopedic assessment
- Duration of symptoms at least three months
You may not qualify if:
- History of shoulder fracture dislocation or surgical intervention
- Neurological disorders affecting shoulder function such as cervical radiculopathy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department of physical therapy,Green international university,Lahore.
Lahore, Punjab Province, 55150, Pakistan
Related Links
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Dr. Fahad Tanveer, DPT,MSPT,PHD
Green International University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- Outcome assessors will be blinded to group allocation to minimize assessment bias. Due to the nature of the intervention (tele-rehabilitation and self-administered exercises), participants and intervention providers will not be blinded.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal investigator
Study Record Dates
First Submitted
May 13, 2026
First Posted
May 28, 2026
Study Start
January 1, 2025
Primary Completion
March 5, 2026
Study Completion
May 10, 2026
Last Updated
May 28, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share
"IPD will not be shared due to participant confidentiality, ethical restrictions, and lack of consent for public data sharing."