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Action Observation Therapy in Patients Undetgoing Surgery for Shoulder Instability

Effects of Action Observation Therapy in Patients Undergoing Surgery for Shoulder-instability

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05479539
Enrollment
40
Registered
2022-07-29
Start date
2022-09-01
Completion date
2023-09-01
Last updated
2022-07-29

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

Conditions

Shoulder Instability

Brief summary

The study will aim at investigating the effects of action observation therapy (action observation plus motor imagery) in patients with shoulder instability undergoing capsulo-plastic surgery. Forty subjects scheduled for capsulo-plastic surgery will be randomized into an AOT or Control group. AOT group will undergo action observation followed by motor imagery of upper limb motor tasks for 4 weeks after surgery, whereas Control group will perform no intervention. In addition, both groups will undergo postoperative usual care including immobilization with a brace and passive upper limb mobilization. All participants will be assessed for shoulder pain, function, range of motion, fear of movement and quality of life the day before surgery, at training end and 3 months after training end.

Interventions

BEHAVIORALAction observation therapy

Participants will watch 12-minute video-clips followed by 8 minutes of motor imagery. Video-clips observation and imagination will be focused un shoulder tasks occuring on the three planes of motion.

Sponsors

Istituto Clinico Humanitas
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

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

Inclusion criteria

* Subjects undergoing capsule-plastic surgery or Latarjet stabilization for shoulder instability

Exclusion criteria

* Previous upper limb surgery * Cognitive impairments * Visual or auditory impairments * Postoperative complications limiting upper limb motor recovery (e.g., infections)

Design outcomes

Primary

MeasureTime frameDescription
Changes in shoulder functionAt baseline, after 4 weeks of training and at 3 month after the training endSimple shoulder test

Secondary

MeasureTime frameDescription
Changes in shoulder painAt baseline, after 4 weeks of training and at 3 month after the training endNumerical Pain Rating Scale (0 - best outcome, 100 worst outcome)
Changes in shoulder range of motionAt baseline, after 4 weeks of training and at 3 month after the training endFlexion, abduction, inernal and external rotation range of motion assessed using a goniometer
Changes in fear of movementAt baseline, after 4 weeks of training and at 3 month after the training endTampa scale of kinesiophobia
Changes in quality of lifeAt baseline, after 4 weeks of training and at 3 month after the training endShort Form - 36 items

Outcome results

None listed

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