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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
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04359160
Acronym
OFUE
Enrollment
59
Registered
2020-04-24
Start date
2020-05-01
Completion date
2020-11-30
Last updated
2021-01-14

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

Conditions

Rotator Cuff Injuries

Keywords

Mobile App, Rotator Cuff, Outpatient surgery, Follow-up

Brief 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.

Interventions

DEVICEOrthense, Orthense, Digikare Inc. Blagnac, France

Mobile-app follow-up care, with questions and score

OTHERQuestionnaire

Paper questionnaire follow-up, with questions and score

Sponsors

L'Institut de Recherche en Chirurgie Orthopédique et Sportive
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

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

Inclusion criteria

* Patients undergoing rotator cuff surgery. They must be able to use a mobile-app, and have an email address and internet connexion.

Exclusion criteria

* Unable to read French

Design outcomes

Primary

MeasureTime frameDescription
Return rate6 weeks postoperativeThe overall response rate to the questionnaires

Secondary

MeasureTime frameDescription
The quality of the responses6 weeks postoperativeresponse rate inside the questionnaire
Net Promoter Score (NPS)6 weeks postoperativewhether or not the patient recommended the questionnaire used, a scale of 0 (not at all likely) to 10 (very likely)
Overall patient satisfaction6 weeks postoperativewhether or not the patient is satisfied of the questionnaire used, a scale of 0 (not at all) to 10 (very good)

Countries

France

Outcome results

None listed

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