Predictors of Recovery Expectancy

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

202 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-03-01

Study Completion Date

2022-02-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of this study is to identify factors that influence a person's expectations regarding recovery from pelvic organ prolapse surgery. This is important because a person's expectations regarding recovery from surgery help to predict how a person will actually recover. Our hypothesis is that women with multiple roles will have expectations of a longer surgical recovery time after surgery for pelvic organ prolapse after controlling for known predictors of recovery expectancies. Participants will complete a preoperative online survey. Additional online surveys will be send on postoperative days 14 and 42 to measure postdischarge surgical recovery.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Caregiver Support and Post-operative Convalescence

NCT04897061

Pelvic Organ Prolapse

COMPLETED

Pelvic Floor Exercise Before Surgery in Women With Pelvic Organ Prolapse

NCT03064750

Pelvic Organ Prolapse Pelvic Floor Disorders

COMPLETED NA

Restricted Convalescence: Outcomes Following Urogynecologic Procedures

NCT02138487

Pelvic Organ Prolapse

COMPLETED NA

Quality of Life After Conservative and Surgical Treatment of Pelvic Organ Prolapse

NCT04110821

Pelvic Organ Prolapse Quality of Life Incontinence

RECRUITING

Postoperative Return to Sexual Activity

NCT05342090

Sexual Function Disturbances Pelvic Organ Prolapse Stress Urinary Incontinence +1 more

COMPLETED NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Pelvic Organ Prolapse Surgery

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Pelvic Organ Prolapse Surgery Patients

Participants with greater than or equal to stage II pelvic organ prolapse who are scheduled for reconstructive surgery will be recruited. Participants will be asked to complete a preoperative online survey regarding their health, recovery expectancy, and different roles. Additional online surveys will be send on postoperative days 14 and 42 to measure postdischarge surgical recovery

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Patients with greater than or equal to stage II pelvic organ prolapse who are scheduled for reconstructive surgery.
* English speaking.
* Over the age of 18.
* Use email as a form of communication.
* Have a reliable internet connection at home.
* Have a computer/smartphone/tablet at home.

Exclusion Criteria

* Non English speaking patients
* Patients without active email.
* Patients without access to reliable internet connection.
* Patients without access to computer/smartphone/tablet.
* Patients with less than stage II prolapse.

Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No