147 Participants Needed

Methods for Recording Postoperative Pain

MT
Overseen ByMeir T Marmor, MD
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: University of California, San Francisco
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests different methods for tracking pain after surgery. Participants will record their pain levels using a hand-written journal, a smartphone app, or a novel electronic pain recorder device, whenever they choose. The goal is to determine which method collects the most accurate and frequent pain data. The trial seeks individuals who have recently undergone orthopedic surgery and can use one of these methods to report their pain. As an unphased trial, it offers participants the chance to contribute to enhancing pain management techniques after surgery.

Do I need to stop my current medications for this trial?

The trial information does not specify whether you need to stop taking your current medications.

What prior data suggests that these methods for recording postoperative pain are safe?

Research shows that the pain recording methods under study—hand-written pain journals, smartphone apps, and new electronic devices—are generally safe for users.

Hand-written pain journals involve simply using pen and paper. People use them to note their pain levels, similar to writing in a diary. This method is common in healthcare and poses no health risks.

The smartphone app was tested with patients who had surgery. Most found it helpful, though a few felt too unwell to use it. The app sends reminders to record pain, which many users appreciate.

The new electronic pain recorder aims to make tracking pain easier and more accurate. Research on similar devices has shown they work well for monitoring symptoms and have no known safety concerns.

Overall, these methods help users track their pain without adding any health risks.12345

Why are researchers excited about this trial?

Researchers are excited about this trial because it explores innovative ways to record postoperative pain, potentially improving patient care. Unlike traditional methods that rely on verbal reports or simple pain scales, this trial examines three distinct approaches: a hand-written pain journal, a novel electronic pain recorder device, and a smartphone app. Each method offers unique features, such as the convenience and accessibility of a smartphone app, the simplicity and tactile nature of a hand-written journal, and the precision of a dedicated electronic device. By comparing these methods, the trial aims to identify the most effective way for patients to communicate their pain levels, ultimately enhancing pain management strategies after surgery.

What evidence suggests that these methods are effective for recording postoperative pain?

This trial will compare different methods for recording postoperative pain: a smartphone app, a novel electronic pain recorder device, and a hand-written pain journal. Research has shown that using a smartphone app to track pain after surgery is effective. In one study, 90% of patients found the app easy to use and could accurately record their pain. The app also allows doctors to monitor pain in real-time, aiding in better management.

Regarding the new electronic pain recorder device, studies have found that electronic methods can be as effective, or even more so, than traditional ways of tracking pain. Many patients find these electronic devices easy to use and are satisfied with them.

As for the hand-written pain journal, while it is a traditional method, specific evidence does not show it to be superior to electronic methods. However, it remains a simple and accessible way for some patients to track their pain.16789

Who Is on the Research Team?

MT

Meir T Marmor, MD

Principal Investigator

University of California, San Francisco

Are You a Good Fit for This Trial?

This trial is for adults over 18 who've had surgery and are experiencing postoperative pain. Participants must be able to use a smartphone and write by hand. Those with altered mental status, neuropathy causing loss of pain sensation, or inability to press buttons due to physical limitations cannot join.

Inclusion Criteria

I am over 18 years old.

Exclusion Criteria

I have lost feeling in some parts of my body due to nerve damage.
I cannot use my hands to write or press a button.
Patient cannot use a smartphone
See 2 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

1-2 weeks

Treatment

Participants record their pain intensity using one of three methods: a smartphone app, a hand-written journal, or a novel electronic device

Up to 2 weeks

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Hand-written pain journal
  • Novel electronic pain recorder device
  • Smartphone app
Trial Overview The study aims to find the best way to track post-surgery pain levels. It compares three methods: writing in a journal, using a smartphone app, and a new electronic device designed for recording pain. Patients will randomly receive one method and log their pain as often as they wish.
How Is the Trial Designed?
3Treatment groups
Experimental Treatment
Group I: Smartphone appExperimental Treatment1 Intervention
Group II: Novel electronic pain recording deviceExperimental Treatment1 Intervention
Group III: Hand-written pain journalExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of California, San Francisco

Lead Sponsor

Trials
2,636
Recruited
19,080,000+

Citations

Quality of Postoperative Pain Management in Orthopedic ...This integrative review seeks to identify the outcomes of pain management specifically concerning sleep quality and patient satisfaction
Assessing Postoperative Pain in Patients Who Underwent ...The aim of the study is to assess the feasibility and effectiveness of the PainPad device in quantifying in-hospital postoperative pain following TKA with or ...
Improving Pain Self-Efficacy in Orthopedic Surgery Patients ...The outcomes were pain self-efficacy, self-reported preparedness about patient management, and patient satisfaction levels with the educational intervention.
Risk Factors for Increased Postoperative Pain and ...We found a significant association between anxiety, current smoking, psychological conditions, and current opioid use with increased preoperative and ...
The Effect of Patient Education on Pain Level and Fear ...We identified that pain management patient education to orthopedic trauma patients before surgery was effective in decreasing the fear of medical pain.
Multimodal Pain Management After Outpatient Orthopedic ...This prospective randomized study investigates the efficacy of a multimodal postoperative pain regimen compared to a traditional opioid-only pain regimen.
Patient-Reported Opioid Use and Pain After Orthopedic or ...Most (61%) of the prescribed opioid tablets were reported as unused, and 28% of patients reported not using any opioids.
Incidence and associated factors of post-operative pain ...The overall incidence of moderate to severe postoperative pain within the first 24 h after emergency orthopedics surgery was 70.5% (95% CI: 64, 77). On ...
results of a prospective randomized controlled trialAs standard of care, patients undergoing shoulder arthroplasties receive written information on their postoperative pain management plan, and a ...
Unbiased ResultsWe believe in providing patients with all the options.
Your Data Stays Your DataWe only share your information with the clinical trials you're trying to access.
Verified Trials OnlyAll of our trials are run by licensed doctors, researchers, and healthcare companies.
Terms of Service·Privacy Policy·Cookies·Security