Trials / Active Not Recruiting
Active Not RecruitingNCT04472117
PREPARE: Patient Centered Perioperative Experience
- Status
- Active Not Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 300 (estimated)
- Sponsor
- Memorial Sloan Kettering Cancer Center · Academic / Other
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine whether an educational video about patients' perioperative experience (period that spans from the time of admission to the hospital to the time of recovery after surgery) will affect the timing of hospital discharge. The researchers will use information collected during this study to create a questionnaire and an educational video related to the patient perioperative experience. The educational video will address patient concerns about the perioperative period and recovery after surgery (post-operative recovery). All participants in this study will be undergoing a MIS hysterectomy according to their routine care in the Gynecology
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | usual care | Interviews will be conducted in person or by telephone by an MD on the research team who does not have an ongoing treatment relationship with the patient, and has been trained by the qualitative methods specialist. Interviews will take place over the phone or in person and are anticipated to last approximately 20-30 minutes. |
| OTHER | Educational video | Watch an educational video created by the research team and.will also complete the post-video survey. Those randomized to view the video must complete the post-video survey (Appendix 3), and all patients must complete the Post-Op Survey with the Patient Experience and Decision Regret Scale (Appendix 5) to be evaluable. If not completed, they will be replaced. |
Timeline
- Start date
- 2020-07-09
- Primary completion
- 2026-07-01
- Completion
- 2026-07-01
- First posted
- 2020-07-15
- Last updated
- 2025-06-04
Locations
7 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT04472117. Inclusion in this directory is not an endorsement.