Evidence map›Paper›PMID 38762720›Full record

ArticleTrials2024

Duloxetine and cognitive behavioral therapy with phone-based support for the treatment of chronic musculoskeletal pain: study protocol of the PRECICE randomized control trial.

Dennis C Ang, Swetha Davuluri, Sebastian Kaplan, Francis Keefe, Christine Rini, Christopher Miles, Haiying Chen

Registry-linked trialAbstract readClinical Trial Protocol
In one paragraph

Article in Trials, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04395001 (Pain Response Evaluation of a Combined Intervention to Cope Effectively), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04395001 phase4completednot on this map

Pain Response Evaluation of a Combined Intervention to Cope Effectively (PRECICE)

TypeinterventionalSponsorWake Forest University Health SciencesRan2021 to 2024Enrolled280ConditionsChronic PainArmsduloxetine, Web-based Cognitive Behavioral Therapy (CBT), Nurse-delivered Motivational Interviewing
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Dennis C AngDepartment of Medicine/Rheumatology, Wake Forest University School of Medicine, Winston Salem, NC, 27157, USA. dang@wakehealth.edu.
Swetha DavuluriDepartment of Psychiatry and Behavioral Medicine, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Sebastian KaplanDepartment of Psychiatry and Behavioral Medicine, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Francis KeefeDepartment of Psychiatry and Behavioral Sciences, Duke University, Durham, NC, USA.
Christine RiniDepartment of Medical Social Sciences, Northwestern University, Chicago, IL, USA.
Christopher MilesDepartment of Family Medicine, Wake Forest University School of Medicine, Winston Salem, NC, USA.
Haiying ChenDepartment of Biostatistical Sciences, Wake Forest University, Winston Salem, NC, USA.

Funding

Pain Response Evaluation of a Combined Intervention to Cope Effectively (PRECICE)UG3NR019196 · NINR · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ANG, DENNIS CHUA · 2020 to 2020
$3.9M
NINR NIH HHS 1UG3NR019196-01NINR NIH HHS UG3 NR019196
6 · The paper itself

Abstract

backgroundChronic musculoskeletal pain (CMP) is the most common, disabling, and costly of all pain conditions. While evidence exists for the efficacy of both duloxetine and web-based cognitive behavioral therapy (CBT) as monotherapy, there is a clear need to consider study of treatment components that may complement each other. In addition, given the reported association between patient's adherence and treatment outcomes, strategies are needed to enhance participant's motivation to adopt and maintain continued use of newly learned pain coping skills from CBT.

methodsTwo hundred eighty participants will be recruited from the primary care clinics of a large academic health care system in North Carolina. Participants with CMP will be randomized to one of three treatment arms: (1) combination treatment (duloxetine + web-based self-guided CBT) with phone-based motivational interviewing (MI), (2) combination treatment without phone-based MI, and (3) duloxetine monotherapy. Participants will be in the study for 24 weeks and will be assessed at baseline, week 13, and week 25. The primary outcome is the Brief Pain Inventory (BPI)-Global Pain Severity score, which combines BPI pain severity and BPI pain interference. Secondary measures include between-group comparisons in mean BPI pain severity and BPI pain interference scores. Data collection and outcome assessment will be blinded to treatment group assignment. DISCUSSION: This randomized controlled trial (RCT) will determine if combination treatment with duloxetine and web-based CBT is superior to duloxetine monotherapy for the management of CMP. Furthermore, this RCT will determine the effectiveness of phone-based motivational interviewing in promoting the continued practice of pain coping skills, thereby enhancing treatment outcomes.

trial registrationNCT04395001 ClinicalTrials.gov. Registered on May 15, 2020.

Indexed as

Chronic PainCognitive Behavioral TherapyDuloxetine HydrochlorideMusculoskeletal PainRandomized Controlled Trials as TopicAdaptation, PsychologicalAdultAnalgesicsCombined Modality TherapyHumansInternet-Based InterventionMotivational InterviewingPain ManagementPain MeasurementTelephoneTime FactorsAnalgesicsDuloxetine HydrochlorideChronic musculoskeletal painCognitive behavioral therapyDuloxetineMotivational interviewingRandomized controlled trial

Identifiers

PMID38762720
PMCPMC11102257

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.