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NCT06206148 · ClinicalTrials.gov registry record · NA

Comparison of Methods for Recording Post Operative Pain

A NA study of Pain, Postoperative, sponsored by University of California, San Francisco.

Recruiting
Registry status
NA
Development phase
147
Enrollment target
1
Study location

NCT06206148 is a NA study of Pain, Postoperative that is actively recruiting participants, run by University of California, San Francisco. The registered enrollment target is 147 participants, below the 271-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (46% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06206148, a NA study of Pain, Postoperative, is actively recruiting participants, sponsored by University of California, San Francisco.

RECRUITING
Registry status
NA
Development phase
147 participants
Enrollment target
1
Study location

Study 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 Studied

Interventions

  • OTHER Smartphone app
  • DEVICE Given novel electronic pain recording device
  • OTHER Given Hand-written pain journal

Study Locations (1)

California

  • Zuckerberg San Francisco General Hospital - San Francisco

Trial Details

FieldValue
Enrollment Target 147 participants
Start Date 2024-03-01
Est. Completion 2026-06
Phase NA

What the Registry Record Tells You About NCT06206148

The ClinicalTrials.gov registry entry for NCT06206148 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 147 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 271-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (46% lower). The listed sponsor is University of California, San Francisco, which has 1,713 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Pain, Postoperative appearing as the primary indexed condition, and to 3 interventions - of which Smartphone app is the first listed.

NCT06206148 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT06206148 about?

NCT06206148 is a clinical study titled "Comparison of Methods for Recording Post Operative Pain". 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 met...

What is the current status of trial NCT06206148?

This trial is currently recruiting. It is a NA study. The enrollment target is 147 participants. The study started on 2024-03-01. Estimated completion is 2026-06.

What conditions does trial NCT06206148 study?

This clinical trial studies the following conditions: Pain, Postoperative.

What interventions are being tested in trial NCT06206148?

The interventions under investigation include: Smartphone app (OTHER), Given novel electronic pain recording device (DEVICE), Given Hand-written pain journal (OTHER).

Who is sponsoring clinical trial NCT06206148?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06206148 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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