Patients Decision-making in Rotator Cuff Surgery

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

80 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-07-07

Study Completion Date

2014-12-29

Brief Summary

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The objective of this study was to evaluate the effect on patient treatment decision-making if information was given based on the benefit or on the side effect in rotator cuff disorders.

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Detailed Description

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Conditions

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Rotator Cuff Disease

Study Design

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Observational Model Type

CASE_CROSSOVER

Study Time Perspective

PROSPECTIVE

Study Groups

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group A (benefit-inform)

filling questionnaire based on benefits of surgery

questionnaire

Intervention Type OTHER

fulfillment of questionnaire

group B (side effect-inform)

filling questionnaire based on side-effects of surgery

questionnaire

Intervention Type OTHER

fulfillment of questionnaire

Interventions

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questionnaire

fulfillment of questionnaire

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* patients diagnosed with rotator cuff tears at their first clinical visit

Exclusion Criteria

* patients with a previous shoulder surgery, patients with worker's compensation and patients who were unwilling to participate and thereby not sign informed consent

Minimum Eligible Age

18 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No