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Comparison of Methods for Recording Post Operative Pain

University of California, San Francisco · NCT06206148

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 18+ · All sexes
Healthy volunteers
Accepted
Study type
Interventional · Not applicable
Target enrollment
147
US sites recruiting
1
Study start
March 1, 2024
Record last updated
July 14, 2025

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

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.

Being studied: Given novel electronic pain recording device; Given Hand-written pain journal; Smartphone app

Conditions: Pain, Postoperative

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • Patient over 18 years old

Exclusion Criteria

  • Patient cannot use a smartphone
  • Patient cannot use his hands to write or press a button
  • Patient has a nerve catheter (has no pain)
  • Altered mental status
  • Neuropathy causing loss of pain sensation

Recruiting US locations

  • Zuckerberg San Francisco General Hospital

    San Francisco, CA 94110

    Site contact: Meir T Marmor, MD · 650-477-6238 · meir.marmor@ucsf.edu

Study contacts (from the official record)

  • Meir T Marmor, MD · 6504776238 · meir.marmor@ucsf.edu
All healthy volunteers studies in California →
Comparison of Methods for Recording Post Operative Pain (NCT06206148) | Bored Studies