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Follow-app intervention arm for Postoperative Complications (AHRQPRO Trial)

N/A
Waitlist Available
Led By Elsbeth Kalenderian, DDS, PhD
Research Sponsored by University of California, San Francisco
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2nd quarter year 3
Awards & highlights

AHRQPRO Trial Summary

This study is evaluating whether a text message based system can help dentists manage pain after hours.

Eligible Conditions
  • Postoperative Complications
  • Postoperative Pain

AHRQPRO Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2nd quarter year 3
This trial's timeline: 3 weeks for screening, Varies for treatment, and 2nd quarter year 3 for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Pain experience in both arms, measured using the American Pain Society, the Patient Outcome Questionnaire (APS-POQ-R) questionnaire.
Pain
Provider Acceptance of FollowApp.Care
Secondary outcome measures
Unscheduled/emergency visits during the study period;

AHRQPRO Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Follow-app intervention armExperimental Treatment1 Intervention
This arm will comprise of patients who are prompted to complete the PROMIS pain intensity scale through text/Short Message Service(SMS) or email mobile device notifications at pre-defined time intervals on Days 1, 3, 5 and 7 post-operatively.
Group II: Standard care armActive Control1 Intervention
This arm will comprise of patients who receive the usual care.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Follow-app intervention arm
2020
N/A
~1530

Find a Location

Who is running the clinical trial?

Agency for Healthcare Research and Quality (AHRQ)FED
399 Previous Clinical Trials
6,820,823 Total Patients Enrolled
University of California, San FranciscoLead Sponsor
2,500 Previous Clinical Trials
15,234,946 Total Patients Enrolled
4 Trials studying Postoperative Complications
572 Patients Enrolled for Postoperative Complications
Elsbeth Kalenderian, DDS, PhDPrincipal InvestigatorUniversity of California, San Francisco

Frequently Asked Questions

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Recent research and studies
clinicaltrials.govStudy
Optimizing Acute Post-Operative Dental Pain Management Using New Health Information Technology
2020. "Optimizing Acute Post-Operative Dental Pain Management Using New Health Information Technology". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT03881891.
~295 spots leftby Apr 2025
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