Impact of an Improved Rehabilitation Program After a Scheduled Hysterectomy.

  • STATUS
    Recruiting
  • participants needed
    148
  • sponsor
    Centre Hospitalier Régional Metz-Thionville
Updated on 19 February 2024
hysterectomy
rehabilitation program

Summary

It is an observational study, prospective in order to assess the impact of the implementation of an early rehabilitation program on post-operative recovery. this is measured by the qOR15 questionnaire in patients operated on for a programmed hysterectomy, it takes place in the gynecology department of the CHR Metz-Thionville hospital.

Description

This program implemented will comply with HAS recommendations. The only change in management for patients participating in the study is the completion of the self-questionnaire QOR-15 on D-1 (the day before the operation), D0 (the day of the operation) and D1 (the day after the operation).

It is planned to include 74 patients before the implementation of the early rehabilitation protocol and 74 patients after the implementation of the early rehabilitation protocol. The total duration of inclusion is established at 18 months.

The measures applied should improve the patient's well-being and accelerate his return to normal life and therefore reduce the length of his stay.

Details
Condition Postoperative Complication
Age 18-100 years
Clinical Study IdentifierNCT04268576
SponsorCentre Hospitalier Régional Metz-Thionville
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Indication of a scheduled hysterectomy
Presence of a utero-ovarian affection, deemed resectable and requiring a regulated hysterectomy (outside the context of the emergency) associated or not with pelvic or lumbar-aortic dissection
classified ASA 1 to 3
informed about the principles of improved rehabilitation by the surgeon and the anesthesiologist + written document (accessible on the site [www.grace-asso.fr](http://www.grace-asso.fr/))
able to return home after discharge from the hospital, having a telephone and being able to contact their doctor or the service if necessary or transferred to a convalescent home at their request

Exclusion Criteria

Patients included in another study
Refusal to use data by the patient
Inability to respond to self-questionnaires due to cognitive impairment, difficulties in reading or understanding the French language
Patients included in another study
Patients with severe or unbalanced associated conditions
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