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NCT07458711
Comparative Effects of Spencer Techniques and Movement With Mobilization in Improving Pain, Range of Motion, and Functional Disability in Rotator Cuff Syndrome.
NA trial testing Spencer technique in Rotator Cuff Syndrome in 60 participants. Completed in 3 March 2026.
28 February 2026
Quick facts
| Lead sponsor | University of Lahore |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 60 |
| Start date | 26 September 2025 |
| Primary completion | 28 February 2026 |
| Estimated completion | 3 March 2026 |
| Sites | 1 location across Pakistan |
Drugs / interventions tested
- Spencer technique
- Movement with mobilization
- conventional physical therapy
Conditions studied
- Rotator Cuff Syndrome — all drugs for Rotator Cuff Syndrome →
Sponsor
University of Lahore
Who can join
Adults 30 to 60, any sex, with Rotator Cuff Syndrome. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This study will be randomised clinical trial conducted at the University of Lahore Teaching Hospital, Lahore, Pakistan. A total of 60 participants will be selected and randomly allocated into two treatment groups (30 participants in each group) using the lottery method. All screened and willing participants who meet the eligibility criteria will be assigned to either Group A or Group B. Group A: Spencer Technique with Conventional Therapy Participants allocated to Group A will receive the Spencer Technique in combination with conventional physiotherapy. The intervention will follow a structured and progressive protocol for 6 weeks. Conventional Therapy (15 minutes per session) Conventional treatment will be administered prior to manual therapy and will include: Moist Hot Pack (5 minutes): A moist hot pack will be applied to the affected shoulder at a comfortable therapeutic temperature. A towel layer will be placed between the hot pack and the skin to prevent burns. Shoulder Stretching Exercises (10 minutes): Passive stretching will be performed to improve flexibility, reduce muscle tightness, and enhance shoulder range of motion. Each stretch will be held for 20-30 seconds and repeated 3-5 times. Stretching will include: Shoulder flexion and extension (supine position) Shoulder abduction Shoulder adduction (cross-body stretch) Internal and external rotation at 90° abduction Stretching will be performed five sessions per week. Spencer Technique (20 minutes per session) Following conventional therapy, the Spencer technique will be administered in seven sequential steps: Shoulder extension with elbow flexion to the point of restriction Shoulder flexion with elbow extension Circumduction with compression at 90° abduction Circumduction with distraction at 90° abduction Abduction with internal rotation (hand placed behind hip) Adduction with external rotation Stretching with fluid pumping maneuver (5-10 repetitions) Dosage and Progression: Frequency: 5 sessions per week Weeks 1-3: 2 sets of 10 repetitions per step (1-minute rest between sets) Weeks 4-6: 3 sets of 10 repetitions per step Total session duration: 35 minutes 5 minutes hot pack 10 minutes stretching 20 minutes Spencer technique Group B: Mobilization with Movement (MWM) with Conventional Therapy Participants allocated to Group B will receive Mobilization with Movement combined with conventional physiotherapy for 6 weeks. Conventional Therapy (15 minutes per session) The same conventional therapy protocol as Group A will be administered prior to mobilization: 5 minutes moist hot pack 10 minutes passive shoulder stretching Mobilization with Movement (20 minutes per session) MWM will be performed in the directions of: External rotation Internal rotation Abduction Flexion The participant will be positioned in sitting on a high chair. The therapist will stabilize the shoulder girdle with one hand while applying a sustained glide to the humeral head using the thenar eminence of the other hand. The glide will be maintained perpendicular to the plane of movement and adjusted according to the participant's pain-free direction. Participants will be instructed to actively move the shoulder through the available range while the glide is sustained. Movement will continue until the onset of pain or discomfort. Dosage: 3 sets of 10 repetitions 30-second rest between sets Frequency: 3 sessions per week Duration: 6 weeks Total session duration: 35 minutes 5 minutes hot pack 10 minutes stretching 20 minutes mobilization with movement
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT07458711
- Europe PMC full search
- ASCO Meeting Library
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Related trials
Other recruiting trials for Rotator Cuff Syndrome
Currently open trials in the same condition.
- NCT07294729 — Mulligan and Proprioceptive Neuromuscular Facilitation Techniques in Individuals With Rotator Cuff Lesions · NA · active not recruiting
- NCT07183774 — Does Sarcopenia Influence Rotator Cuff Tear Patterns? Radiological Insights From Patients With Rotator Cuff Syndrome · recruiting
- NCT06228625 — Comparison of Rehabilitative Game Exercise and Body Awareness Therapy in Rotator Cuff Syndrome · NA · recruiting
- NCT06723730 — ADDITIONAL EFFECTS OF MOBILIZATION WITH MOVEMENT WITH UPPER QUADRANT CORE STRENGTHENING IN ROTATOR CUFF RELATED PAIN:A R · NA · recruiting
Other University of Lahore trials
Trials by the same sponsor.
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- NCT07446218 — Pharmacist-led Interventions in Psychiatric Patients · NA · not yet recruiting
- NCT07359378 — Progressive Resistance Exercise Versus Functional Training in Elderly With Risk of Fall. · NA · not yet recruiting
- NCT07244913 — Therapeutic Effects of Instrument-assisted Versus Sound-assisted Soft Tissue Mobilization in Chronic Non-specific Low Ba · NA · recruiting
- NCT07436624 — Kabat Rehabilitation Versus Kinesiology Taping in Bell's Palsy · NA · active not recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT07458711 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by University of Lahore
- Last refreshed: 9 March 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07458711.
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