Comparison of Methods for Recording Post Operative Pain
NCT06206148 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 147
Last updated 2025-07-14
Summary
The purpose of the current study is to identify the optimal method of collection of pain intensity data. The study will compare three collection methods: a hand-written pain journal, a smartphone app, and a novel electronic pain recorder device. Patients will be randomly assigned to one of three methods and instructed to record their pain level as often as they like. The number of pain intensity recordings per day will then be compared across groups.
Conditions
- Pain, Postoperative
Interventions
- DEVICE
-
Given novel electronic pain recording device
Patients in this arm will be given a custom-built pain recording device to see if the method of self-reported data collection has any effect on how many data points are collected.
- OTHER
-
Given Hand-written pain journal
Patients in this arm will be given a hand-written pain journal to see if the method of self-reported data collection has any effect on how many data points are collected.
- OTHER
-
Smartphone app
Patients in this arm will be given a research smartphone with survey app to see if the method of self-reported data collection has any effect on how many data points are collected.
Sponsors & Collaborators
-
University of California, San Francisco
lead OTHER
Principal Investigators
-
Meir T Marmor, MD · University of California, San Francisco
Study Design
- Allocation
- RANDOMIZED
- Purpose
- DIAGNOSTIC
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2024-03-01
- Primary Completion
- 2026-06-30
- Completion
- 2026-06-30
- FDA Device
- Yes
Countries
- United States
Study Locations
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