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NCT03764839 · ClinicalTrials.gov registry record · NA
Digital Behavioral Pain Medicine for Orthopedic Trauma Surgery Patients
A NA study, sponsored by Stanford University.
- Completed
- Registry status
- NA
- Development phase
- 141
- Enrollment target
NCT03764839: Completed NA study, sponsored by Stanford University.
NCT03764839 is a NA study that has completed, run by Stanford University. The registered enrollment target is 141 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03764839, a NA study, has completed, sponsored by Stanford University.
- COMPLETED
- Registry status
- NA
- Development phase
- 141 participants
- Enrollment target
Study Summary
The primary purpose of this study is to determine the feasibility and preliminary efficacy of a perioperative digital behavioral pain medicine intervention delivered to orthopedic trauma surgery patients (compared to an active control group that receives digital health education). Aim 1: Determine feasibility of and satisfaction, and perceived utility of "My Surgical Success" Hypothesis 1: For My Surgical Success, the investigators anticipate 50% engagement in the study (feasibility). Of those who complete My Surgical Success, the investigators expect 80% satisfaction ratings, and 80% perceived utility of the information learned. Aim 2: Determine group differences in time to post-surgical pain and opioid cessation. Hypothesis 2: "My Surgical Success" participants will evidence quicker time to post-surgical pain and opioid cessation compared to the HE Control Group. Aim 3: Determine group differences in within-subject pain catastrophizing scores (baseline to post-surgery). Hypothesis 3: "My Surgical Success" participants evidence greater reduction in pain catastrophizing (measured with the Pain Catastrophizing Scale; PCS) compared to the HE Control group. Aim 4: Determine group differences in post-surgical psychological correlates (PROMIS Depression, Anxiety, Function, Pain Interference, Sleep Disturbance, Social Isolation, Fatigue, and Pain Intensity). Hypothesis 4: "My Surgical Success" participants will evidence greater post-surgical function and lower pain related interference compared to the HE Control Group. The goal of this research is to advance our understanding regarding the feasibility and effectiveness of "My Surgical Success" (a digital, perioperative behavioral pain medicine treatment) and its impact on post-surgical outcomes.
Primary Outcome
Participants complete a single time point rating for 5 items listed above. Ratings occur on a 0-6 point scale (e.g., 0=completely useless and 6=Very useful). Percentages will be reported for each item. A higher score indicates better acceptability, satisfaction, usefulness of the information.
Interventions
- BEHAVIORAL Perioperative Digital Behavioral Pian Medicine "My Surgical Success"
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 141 participants |
| Start Date | 2018-10-05 |
| Est. Completion | 2020-04-05 |
| Phase | NA |
What the finished NCT03764839 record still lists
NCT03764839 is an interventional study that assigns participants to a tested intervention. The registered 141 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower).
The record links to 0 conditions, and to 1 intervention - of which Perioperative Digital Behavioral Pian Medicine "My Surgical Success" is the first listed.
NCT03764839 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03764839 about?
NCT03764839 is a clinical study titled "Digital Behavioral Pain Medicine for Orthopedic Trauma Surgery Patients". The primary purpose of this study is to determine the feasibility and preliminary efficacy of a perioperative digital behavioral pain medicine intervention delivered to orthopedic trauma surgery patients (compared to an active control group that receives digital health education). Aim 1: Determine ...
What is the current status of trial NCT03764839?
This trial is currently completed. It is a NA study. The enrollment target is 141 participants. The study started on 2018-10-05. Estimated completion is 2020-04-05.
What interventions are being tested in trial NCT03764839?
The interventions under investigation include: Perioperative Digital Behavioral Pian Medicine "My Surgical Success" (BEHAVIORAL).
Who is sponsoring clinical trial NCT03764839?
This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03764839's enrollment target sits among peer trials
141 712th of 2000 higher than 1,288 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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