Evidence map›Paper›PMID 39706331›Full record

ArticleContemporary clinical trials2025

Web-Based Pain Coping Skills Training (PCST) for Managing Aromatase Inhibitor-Associated Arthralgia in Breast Cancer Survivors: Randomized Controlled Trial Protocol.

Zahra Hosseinian, Ashley Lehan, Jessica M Powers, Adrian Melendez, Hannah M Fisher, Rebecca Shelby, Tamara Somers, Francis Keefe, Judith Paice, Gretchen Kimmick and 7 more

Abstract readClinical Trial Protocol
In one paragraph

Article in Contemporary clinical trials, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Zahra HosseinianDepartment of Medical Social Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL, United States of America.
Ashley LehanDepartment of Medical Social Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL, United States of America.
Jessica M PowersDepartment of Medical Social Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL, United States of America.
Adrian MelendezDepartment of Medical Social Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL, United States of America.
Hannah M FisherDepartment of Psychiatry and Behavioral Sciences, Duke University, Durham, NC, United States of America.
Rebecca ShelbyDepartment of Psychiatry and Behavioral Sciences, Duke University, Durham, NC, United States of America.
Tamara SomersDepartment of Psychiatry and Behavioral Sciences, Duke University, Durham, NC, United States of America.
Francis KeefeDepartment of Psychiatry and Behavioral Sciences, Duke University, Durham, NC, United States of America.
Judith PaiceDepartment of Medicine (Hematology and Oncology), Northwestern University Feinberg School of Medicine, Chicago, IL, United States of America.
Gretchen KimmickDepartment of Medicine, Duke University, Durham, NC, United States of America.
James BurnsDepartment of Medical Social Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL, United States of America.
Ann Marie FloresDepartment of Medical Social Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL, United States of America; Department of Physical Therapy and Human Movement Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL, United States of America; Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL, United States of America.
Rina S FoxUniversity of Arizona College of Nursing, Division of Advanced Nursing Practice and Science, Tuscon, AZ, United States of America.
Karen KaiserDepartment of Medical Social Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL, United States of America.
David FarrellPeople Designs, Inc., Durham, NC, United States of America.
Kelly WestbrookDepartment of Medicine, Duke University, Durham, NC, United States of America; Duke Cancer Institute, Duke University Medicine Center, Durham, NC, United States of America.
Christine RiniDepartment of Medical Social Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL, United States of America; Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL, United States of America. Electronic address: Christine.rini@northwestern.edu.

Funding

Cancer Prevention, Control, and Survivorship Research Training ProgramT32CA193193 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Brian L Hitsman, BETINA YANEZ · 2015 to 2026
$3.8M
Web-based Pain Coping Skills Training to Improve Pain and Poor Adherence caused by Aromatase Inhibitor-Associated Arthralgia In Breast Cancer Survivors (SKIP-Arthralgia): A Randomized Controlled TrialR01CA271220 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Christine Rini · 2022 to 2026
$3.2M
NCI NIH HHS R01 CA271220NCI NIH HHS T32 CA193193
6 · The paper itself

Abstract

backgroundAromatase inhibitors (AIs) are a cornerstone of adjuvant systemic therapy for postmenopausal patients with hormone-receptor positive (HR+) breast cancer. Although AIs decrease cancer recurrence rates and improve survival rates, approximately 50 % of patients experience arthralgia-persistent pain related to worse patient outcomes and poor AI adherence. Current medical interventions for AI-associated arthralgia have limited efficacy and side effects that restrict their use among older patients.

objectiveThe SKIP-Arthralgia trial will test the efficacy of Pain Coping Skills Training (PCST), a cognitive-behavioral therapy (CBT)-informed intervention, delivered via a web-based program called painTRAINER®. PCST and similar CBT-informed pain interventions are efficacious in non-cancer pain and commonly delivered via the Internet, although they have not been tested as a treatment for AI-associated arthralgia.

methods452 breast cancer survivors with AI-associated arthralgia will complete a baseline assessment before being randomized to either painTRAINER plus enhanced usual care (EUC; educational materials about AI therapy, arthralgia, and pain), or to EUC alone. Follow-up assessments will occur approximately 2 weeks after the 8- to 10-week intervention period (post-intervention) and at 3- and 6-months post-intervention. Primary outcomes are pain severity and interference at post-intervention. Secondary outcomes include emotional distress, AI adherence, and health-related quality of life. DISCUSSION: This trial aims to fill a gap in evidence-based behavioral pain interventions for breast cancer survivors with AI-associated arthralgia by providing an effective, accessible intervention that could be implemented quickly, including in areas with limited PCST access. If successful, this study could enhance health outcomes for breast cancer survivors on AI therapy and improve adherence to this life-saving medication.

Indexed as

Adaptation, PsychologicalAromatase InhibitorsArthralgiaBreast NeoplasmsCancer SurvivorsCognitive Behavioral TherapyCoping SkillsFemaleHumansInternet-Based InterventionQuality of LifeRandomized Controlled Trials as TopicAromatase InhibitorsAromatase inhibitorsArthralgiaBreast cancerCancer painCognitive-behavioral therapyDigital healthPain

Identifiers

PMID39706331
PMCPMC12257631

What OpenQuestion holds

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Registered trials

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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.