Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT02771964 · ClinicalTrials.gov registry record
Assessing Change in Patient-reported Quality of Life After Elective Surgery: an Observational Comparison Study
A clinical trial, sponsored by Washington University School of Medicine.
- Completed
- Registry status
- 17,850
- Enrollment target
NCT02771964: Completed study, sponsored by Washington University School of Medicine.
NCT02771964 is a clinical trial that has completed, run by Washington University School of Medicine. The registered enrollment target is 17,850 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02771964 has completed, sponsored by Washington University School of Medicine.
- COMPLETED
- Registry status
- 17,850 participants
- Enrollment target
Study Summary
This study will compare two commonly-used methods for assessing patient-reported quality of life. The first is to assess quality of life before surgery and again after surgery using the same validated scale (ie Veterans Rand 12). The second is simply to ask patients whether or not they think their post-operative quality of life is better, worse, or the same. The investigators hypothesize that the second method may be inaccurate due to cognitive bias.
Interventions
- OTHER Quality of life survey
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 17,850 participants |
| Start Date | 2014-01 |
| Est. Completion | 2016-07 |
What the finished NCT02771964 record still lists
NCT02771964 is an observational study that tracks outcomes without assigning an intervention. Its 17,850 participants enrollment target places it among the larger protocols in the corpus.
The record links to 0 conditions, and to 1 intervention - of which Quality of life survey is the first listed.
NCT02771964 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02771964 about?
NCT02771964 is a clinical study titled "Assessing Change in Patient-reported Quality of Life After Elective Surgery: an Observational Comparison Study". This study will compare two commonly-used methods for assessing patient-reported quality of life. The first is to assess quality of life before surgery and again after surgery using the same validated scale (ie Veterans Rand 12). The second is simply to ask patients whether or not they think their p...
What is the current status of trial NCT02771964?
This trial is currently completed. The enrollment target is 17,850 participants. The study started on 2014-01. Estimated completion is 2016-07.
What interventions are being tested in trial NCT02771964?
The interventions under investigation include: Quality of life survey (OTHER).
Who is sponsoring clinical trial NCT02771964?
This trial is sponsored by Washington University School of Medicine, which has 1,502 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT07108660 · 17,800 participants · NA
Machine Learning Prediction of Possible Central Line Associated Blood Stream Infections and Rate of Reduction
- NCT04110522 · 18,000 participants · NA
Psoriatic Arthritis D2P Screening
- NCT05513833 · 18,000 participants · NA
School Screening and Telemedicine Specialty Referral to Address Childhood Hearing Loss in Rural Kentucky
- NCT06802224 · 18,000 participants · Phase 4
The Choice of Vasopressor to Prevent Postoperative Acute Kidney Injury After Major Non-Cardiac Surgery
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia