Clinical Trials Directory

Trials / Completed

CompletedNCT04897061

Caregiver Support and Post-operative Convalescence

Impact of Home Support on Quality of Post-operative Recovery After Major Pelvic Organ Prolapse Surgery

Status
Completed
Phase
Study type
Observational
Enrollment
103 (actual)
Sponsor
Icahn School of Medicine at Mount Sinai · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is a prospective cohort study designed to investigate the impact of home caregiver support on post-operative convalescence in patients undergoing same day discharge after major urogynecologic surgery. Questionnaires assessing post-operative convalescence will be distributed at several time points after surgery. The main hypothesis is that increased caregiver support in the post-operative period will improve post-operative convalescence of patients undergoing major urogynecologic surgery.

Detailed description

Pelvic organ prolapse and incontinence surgery is now often done on an outpatient basis (also known as same day discharge surgery or SDD). While there are data to support the safety of this practice, little is known about the burden and demands of this practice on the patient and her support system/caregivers. Furthermore, there are no guidelines on requirements for assistance at home or what impact home caregiver support has on recovery. The study team is interested in investigating the spectrum of support that patients have at home in terms of caregivers such as family, friends, neighbors and how that may impact their recovery. The intervention for this study will be comprised of administering post-operative questionnaires that assess patients' post-operative convalescence and quantify the required or available caregiver support. The clinical outcome of interest is recovery as assessed by the validated questionnaires.

Conditions

Timeline

Start date
2021-05-24
Primary completion
2022-11-01
Completion
2022-11-01
First posted
2021-05-21
Last updated
2022-11-22

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04897061. Inclusion in this directory is not an endorsement.