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RECRUITING
NCT06206148
NA

Comparison of Methods for Recording Post Operative Pain

Sponsor: University of California, San Francisco

View on ClinicalTrials.gov

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.

Official title: Comparison of Methods for Recording Post Operative Pain: A Prospective Randomized Trial

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

147

Start Date

2024-03-01

Completion Date

2026-06

Last Updated

2025-07-14

Healthy Volunteers

Yes

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.

Locations (1)

Zuckerberg San Francisco General Hospital

San Francisco, California, United States