Comparison of Methods for Recording Post Operative Pain - Trial NCT06206148
Access comprehensive clinical trial information for NCT06206148 through Pure Global AI's free database. This phase not specified trial is sponsored by University of California, San Francisco and is currently Not yet recruiting. The study focuses on Pain, Postoperative. Target enrollment is 147 participants.
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Study Focus
Sponsor & Location
University of California, San Francisco
Timeline & Enrollment
N/A
Mar 01, 2024
Jun 01, 2024
Primary Outcome
Comparing Methods for Pain Score collection
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.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT06206148
Device Trial