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Early Active Rehabilitation After Arthroscopic Rotator Cuff Repair

Early Active Rehabilitation After Arthroscopic Rotator Cuff Repair: A Prospective Randomized Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02915588
Enrollment
30
Registered
2016-09-27
Start date
2012-01-31
Completion date
2013-12-31
Last updated
2016-09-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Full Thickness Rotator Cuff Tear

Brief summary

The purpose of the study is to compare two different rehabilitation protocols after arthroscopic rotator cuff surgery.

Interventions

OTHERearly isometric loading after rotator cuff surgery
OTHERpassive motion after rotator cuff surgery

Sponsors

Johannes Kepler University of Linz
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* surgery of the rotator cuff after full thickness tear * informed consent * understanding german language

Exclusion criteria

* previous surgery of the shoulder * neurological or systemic diseases with impairment of shoulder function

Design outcomes

Primary

MeasureTime frameDescription
Change of Constant Murley Scoreup to 24 weeksTimepoints: Before surgery; 6, 12, 24 weeks after surgery

Secondary

MeasureTime frameDescription
Change of DASH Scoreup to 24 weeksTimepoints Before surgery; 6, 12, 24 weeks after surgery
Change of Active range of Motion (Flexion, Extension, Abduction, Internal Rotation, External Rotation)up to 24 weeksTimepoints: Before surgery; 6, 12, 24 weeks after surgery; Range of movement is measured by handheld goniometer
Change of Pain (max; average; rest)up to 24 weeksTimepoints: Before surgery; 6, 12, 24 weeks after surgery; Pain is measured by Visual Analogue Scale (0-100mm)
Change of Strength (abduction; external Rotation)up to 24 weeksTimepoints: Before surgery; 6, 12, 24 weeks after surgery; Measurement of Strength is evaluated using a BTE Simulator II Dynamometer (Peak torque in N).

Countries

Austria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026