Skip to content

The Effect of Exercise Based Management on Multidirectional Instability of the Glenohumeral Joint: A Pilot Randomised Controlled Trial.

The effect of two different exercise programs on scapula, strength and function measures of participants with clinically diagnosed Multidirectional Instability of the glenohumeral joint.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12613001240730
Enrollment
328
Registered
2013-11-12
Start date
2013-11-18
Completion date
2015-11-30
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

The primary purpose of this study is to compare the relative effectiveness of two different and standardised exercise programs (The Lyn Watson Program and The Rockwood Program) on function and instability specific outcomes as well as strength and scapula measures, on patients with non traumatic Multidirectional Instability of the glenohumeral joint. The hypothesis is that the Lyn Watson program will produce clinically and statistically superior results on outcomes due to the program’s focus on achieving and maintaining scapula control.

Interventions

12 physiotherapy sessions (one 60 minute session and eleven 30 minute session one to one) delivering the Lyn Watson MDI Program. This rehabilitation program is primarily based around maintaining good scapula and humeral head control through 6 stages. Assessment of the effect of manual correction determines the position of scapula and/or humeral head control that improves a patient’s objective asterisk(s). This position is then adopted in a ‘setting’ action whist performing drills in the rele

12 physiotherapy sessions (one 60 minute session and eleven 30 minute session one to one) delivering the Lyn Watson MDI Program. This rehabilitation program is primarily based around maintaining good scapula and humeral head control through 6 stages. Assessment of the effect of manual correction determines the position of scapula and/or humeral head control that improves a patient’s objective asterisk(s). This position is then adopted in a ‘setting’ action whist performing drills in the relevant stages. Exercises are performed with theraband or weights for resistance. An outline of the 6 stages of the Lyn Watson protocol is as follows: Stage 1- Coronel Plane Strengthening 0 to 45 degrees Abduction: Scapula upward rotation and tilting Internal Rotation/External Rotation from 0 to 45 abduction with theraband Standing/bent over rows 0 to 45 degrees abduction Stage 2- Building Posterior Musculature Bent over rows Side lie external rotation Standing rows Stage 3: Flexion Drills Flexion Drills from 0 to 45 degrees Abduction Stage 4: Coronal Plane Strengthening 45 to 90 degrees Abduction Internal Rotation/External Rotation from 45 to 90 degrees abduction with theraband Standing/bent over rows 0 to 45 degrees abduction Flexion to 90 degrees abduction Stage 5: Specific Strength Drills Bent over rows (Posterior deltoid) Supine and sitting flexion (Anterior deltoid) Lateral Raises (Middle deltoid) Stage 6: Sports Specific and Functional Specific Drills Drills determined by the requirements of the patient. Load and progressed to allow for return to sport or function. Each week will be used to review, prescribe and progress the exercise program. A trained trial physiotherapist will deliver the program and compliance will be monitored by exercise log sheets. Each participant will be asked to perform his or her prescribed exercise program at home (home exercise program). This will involve the participant performing 3 to 7 exercises with the use of therabands and weights, which will be provided to the participant as part of the trial. The exercise program will take between 15 and 20 minutes to complete and will be performed two to three times a day; to once every two days, depending on the phase of the program. At the beginning of the program, the exercises will focus more on recruitment of muscle (exercises performed two to three times a day) and later in the program the exercises may focus more on muscle strength (exercises performed once every second day). At the end of the 12 week program and after the 12 week outcome measures have been taken, participants who score less than a minimal detectable change on both primary outcome measures have the option to cross over into the alternative treatment arm for a subsequent 12 weeks.

Sponsors

Health Networks Australia / LifeCare Health
Lead SponsorCommercial sector/Industry

Study design

Allocation
Randomised controlled trial
Intervention model
Other
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
12 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

Diagnosis of MDI (Instability in at least 2 directions). No significant history of trauma Willingness to participate in a 12 week exercise program Aged between 12 and 35 years inclusive. No bony or labral lesion detected on Magnetic Resonance Imaging (MRI) scan.

Exclusion criteria

History of significant trauma Bony or labral lesion detected on MRI Prior surgical history of the affected shoulder (s) Non correctable volitional instability Ehler-Danlos Syndrom/Marfan’s Syndrome Shoulder pain that is predominantly due to cervical pain

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 13, 2026