Trials / Completed
CompletedNCT04359160
Comparison of Follow-up by Mobile App or Paper Questionnaire of Patients Undergoing Rotator Cuff Surgery
Comparison of Follow-up by Mobile Application or Paper Questionnaire of Patients Undergoing Rotator Cuff Surgery: Monocentric, Prospective, Randomized Study
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 59 (actual)
- Sponsor
- L'Institut de Recherche en Chirurgie Orthopédique et Sportive · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study evaluate if in an outpatient rotator cuff surgery, can the use of mobile app compared to conventional paper questionnaire improve follow-up care in the first 90-days following surgery.
Detailed description
Rotator cuff surgery is a painful arthroscopic surgery. In outpatient surgery, the surgeons have to increase the security and surveillance after the surgery to reassure the patient and avoid complications. Most patients receiving ambulatory rotator cuff surgery have high pain score, and management and aspects of the rehabilitation can be challenging. However, regular follow-up is still considered important in the early post-operative phase. In between the conventional appointment 6 weeks post op and 12 weeks post op, the surgeons have no status of the patient, and no markers to check if the postoperative care is evolving right. Currently, the investigators are using a mobile application (Orthense by Digikare, Blagnac, France) to complement in-person postoperative follow-up care for patients.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Orthense, Orthense, Digikare Inc. Blagnac, France | Mobile-app follow-up care, with questions and score |
| OTHER | Questionnaire | Paper questionnaire follow-up, with questions and score |
Timeline
- Start date
- 2020-05-01
- Primary completion
- 2020-11-30
- Completion
- 2020-11-30
- First posted
- 2020-04-24
- Last updated
- 2021-01-14
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT04359160. Inclusion in this directory is not an endorsement.