NCT07482735

Brief Summary

Partial rotator cuff tears negatively affect shoulder stability, proprioception, and neuromuscular control. Perturbation-based rehabilitation has been shown to enhance reflex muscle activation and dynamic joint stabilization; however, randomized controlled studies investigating its effects in patients with partial rotator cuff tears are limited. This single-blind randomized controlled trial aims to investigate the long-term effects of a perturbation exercise protocol on pain, proprioception, muscle strength, range of motion, and functional performance in individuals with partial rotator cuff tears. Sixty participants will be randomly assigned to either a conventional physiotherapy group or a perturbation-based rehabilitation group. Outcomes will be assessed at baseline, post-treatment (10 days), and one month follow-up.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
3mo left

Started Mar 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress61%
Mar 2026Oct 2026

First Submitted

Initial submission to the registry

March 15, 2026

Completed
1 day until next milestone

Study Start

First participant enrolled

March 16, 2026

Completed
3 days until next milestone

First Posted

Study publicly available on registry

March 19, 2026

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2026

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 31, 2026

Expected
Last Updated

March 19, 2026

Status Verified

March 1, 2026

Enrollment Period

5 months

First QC Date

March 15, 2026

Last Update Submit

March 15, 2026

Conditions

Keywords

Partial rotator cuff tearsPerturbation-based rehabilitationProprioceptionMuscle strengthFunctional performance

Outcome Measures

Primary Outcomes (1)

  • Shoulder muscle strength

    Shoulder flexor, abductor, and medial and lateral rotator muscles muscle strength measured by Handheld Dynamometer

    Baseline, Day 10 (post-treatment), 1 month follow-up

Secondary Outcomes (5)

  • Shoulder Range of Motion

    Time Frame: Baseline, Day 10 (post-treatment), 1 month follow-up

  • Shoulder Pain

    Baseline, Day 10 (post-treatment), 1 month follow-up

  • Proprioception

    Baseline, Day 10 (post-treatment), 1 month follow-up

  • Functional Status

    Baseline, Day 10 (post-treatment), 1 month follow-up

  • Dynamic balance

    Baseline, Day 10 (post-treatment), 1 month follow-up

Study Arms (2)

Experimental Group

EXPERIMENTAL

Conventional physiotherapy + perturbation exercise protocol

Other: Conventional physiotherapyOther: Perturbation exercise protocol

Control Group

OTHER

Conventional physiotherapy only

Other: Conventional physiotherapy

Interventions

Non

Also known as: Non
Control GroupExperimental Group

Non

Experimental Group

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Age 18-65 years
  • Clinically diagnosed partial rotator cuff tear
  • Suitable for physiotherapy
  • Signed informed consent

You may not qualify if:

  • Full-thickness rotator cuff tear
  • Previous shoulder surgery
  • History of fracture or dislocation
  • Adhesive capsulitis
  • Neurological deficit in upper extremity
  • Professional athletes
  • Active systemic rheumatologic disease

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sivas Cumhuriyet University

Sivas, 58140, Turkey (Türkiye)

Location

Study Officials

  • Selvin Balki, Assoc. prof. Dr

    Cumhuriyet University

    STUDY CHAIR
  • Ayşe Nur Engindoğan, MSc

    Cumhuriyet University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Paralel Randomized
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate professor, Ph.D.

Study Record Dates

First Submitted

March 15, 2026

First Posted

March 19, 2026

Study Start

March 16, 2026

Primary Completion

July 31, 2026

Study Completion (Estimated)

October 31, 2026

Last Updated

March 19, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Locations