NCT05531929

Brief Summary

Anxiety-depressive disorders are also very frequent, in the form of different pathologies that are often intertwined (prevalence of generalized anxiety disorders in 5% of the population, characterized depressive episodes in 5%, etc.). And it is even more frequent in patients with a cuff tendinopathy (26% and 23% of depression and anxiety respectively). These 2 pathologies are therefore responsible for significant economic expenses. It is in this context that the investigators' wish to carry out this study seems justified in order to better understand and therefore manage this problem, which is frequently encountered in daily practice and which would therefore allow better understanding and therefore better information for the patients concerned.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
212

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started May 2022

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 22, 2022

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

September 2, 2022

Completed
6 days until next milestone

First Posted

Study publicly available on registry

September 8, 2022

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 22, 2022

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 22, 2022

Completed
Last Updated

December 19, 2023

Status Verified

December 1, 2023

Enrollment Period

5 months

First QC Date

September 2, 2022

Last Update Submit

December 12, 2023

Conditions

Keywords

Anxiety Depression DisorderRotator cuff repair

Outcome Measures

Primary Outcomes (1)

  • Measurement of the duration of complete sports cessation after rotator cuff repair surgery

    6 months after rotator cuff repair surgery

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Major subject (≥ 18 years) operated between January 2008 and September 2009 arthroscopically for a symptomatic supraspinatus tendon rupture

You may qualify if:

  • Major subject (≥ 18 years)
  • Operated between January 2008 and September 2009 arthroscopically for a symptomatic supraspinatus tendon rupture, retracted in zone 1, resistant to medical treatment with a mobile shoulder, fatty degeneration of stage 2 or less with also a preserved subacromial space
  • Subject not objecting to the reuse of their data for scientific research purposes.

You may not qualify if:

  • \- Subject having expressed his opposition to the reuse of his data for scientific research purposes.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Service de Chirurgie orthopédique de l'épaule et du coude - CHU de Strasbourg - France

Strasbourg, 67091, France

Location

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 2, 2022

First Posted

September 8, 2022

Study Start

May 22, 2022

Primary Completion

October 22, 2022

Study Completion

December 22, 2022

Last Updated

December 19, 2023

Record last verified: 2023-12

Locations