Awardee OrganizationUNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON
Description
Abstract Text
PROJECT SUMMARY
Despite a range of therapeutic approaches, chronic musculoskeletal pain (CMP) persists at a high rate, creating a public health burden. Our long-term goal is to increase access and scalability of evidence-based interventions while addressing pain care disparities for rural individuals with limited resources and/or endure long distances to specialty pain care. We will conduct a hybrid implementation-effectiveness trial, guided by the Reach, Effectiveness, Adoption, Implementation, and Maintenance framework in diverse healthcare systems and communities across the United States in Texas and South Carolina focusing on rural health populations. Specifically, in our UG3 phase, we aim to plan and evaluate our Auricular Point Acupressure Self-Management (APA-SM) program integrated into rural health care and communities. Our team has accumulated extensive evidence supporting the use of APA-SM in decreasing pain intensity, reducing pain interference, and improving physical function. To maximize self-management of pain, we successfully developed and tested a smartphone APA app, an integral component of our APA-SM program, so patients can learn to self-administer APA. We also used ecological momentary assessment integrated into our app to measure real-world outcomes with participants able to self-monitor their progress using this as an innovative behavior change strategy. Our APA-SM program is theory-based according to Bandura’s self-efficacy model, toward successful initiation and maintenance of participants’ behavior change.
In the UG3 phase, we will work with the NIH Pragmatic Trials Collaboratory Coordinating Center and collaborate extensively with our stakeholders to plan, implement, evaluate, and sustain our intervention. In the UH3 phase, using a pragmatic, randomized clinical trial, we will evaluate the clinical effectiveness of our 4-week APA-SM program. We will compare 3 groups: self-guided APA-SM, APA-SM + in-person training, and education control. The primary outcomes are pain intensity, pain interference, and function; the secondary outcomes are based on the HEAL Clinical Pain Core common data elements, and analgesic use, up to a 6-month follow-up. We will also evaluate implementation outcomes, cost-effectiveness, and predictive factors for APA-SM treatment response. A two-phase design in our UH3 will include an initiation (support for buy-in) and maintenance (no support provided) phase.
Public Health Relevance Statement
PROJECT NARRATIVE
Chronic pain is a major health concern and places an enormous burden on society and healthcare systems in
the U.S., especially in rural areas. This project aims to plan and test auricular point acupressure self-
management (APA-SM) integrated into primary care. We will conduct a real-world trial to evaluate clinical
effectiveness, implementation outcomes, and cost-effectiveness toward revolutionizing pain management
particularly for rural populations.
NIH Spending Category
No NIH Spending Category available.
Project Terms
AcupressureAcupuncture TherapyAddressAdherenceAdoptedAdultAdvocateAnalgesicsCaringCellular PhoneClinicClinicalClinical ManagementClinical effectivenessCollaborationsCollectionCommon CoreCommon Data ElementCommunitiesComputersCost AnalysisDataDemographic FactorsDisparityEarEcological momentary assessmentEducationEducational process of instructingElectronic Health RecordEligibility DeterminationEnrollmentEnsureEquityEventEvidence based interventionExhibitsFosteringGoalsGuidelinesHeadacheHealthHealth Services AccessibilityHealthcareHealthcare SystemsIndividualInterventionLearningMaintenanceMeasuresMethodsMigraineModelingMonitorMotivationMusculoskeletal PainNonpharmacologic TherapyOutcomePainPain intensityPain interferencePain managementParticipantPatient CompliancePatient PreferencesPatient-Centered CarePatientsPersonsPharmaceutical PreparationsPhasePhysical FunctionPopulation HeterogeneityPredictive FactorPrimary CareProceduresProtocols documentationProviderPublic HealthQuality ControlQuality of lifeRandomizedRandomized, Controlled TrialsReach, Effectiveness, Adoption, Implementation, and MaintenanceRecording of previous eventsReportingResearchResourcesRuralRural HealthRural PopulationSample SizeSelf AdministrationSelf EfficacySelf ManagementSocietiesSouth CarolinaSystemTabletsTestingTexasTherapeuticTimeTrainingUnited StatesUnited States National Institutes of HealthWorkarmbehavior changecancer painchronic musculoskeletal painchronic painchronic pain managementclinical painclinical practicecollaboratorycommunity partnerscomorbiditycomparison controlcost effectivenesscost-effectiveness ratiodesigndigitaldisabilityeffectiveness evaluationeffectiveness outcomeeffectiveness/implementation hybrideffectiveness/implementation trialempowermentevidence baseflexibilityfollow-upgeographic populationhealth care settingshealth equityimplementation costimplementation evaluationimplementation outcomesimprovedincremental cost-effectivenessinnovationmedical specialtiesopioid epidemicopioid usepain outcomepain reductionpain self-managementpatient health informationpilot testpopulation healthpragmatic trialprimary care settingprimary outcomeprogramsrandomized, clinical trialsrecruitresponseroutine carerural arearural disparitiesrural healthcaresatisfactionsecondary outcomeself-management programskillsstatistical and machine learningtheoriestreatment as usualtreatment response
National Center for Complementary and Integrative Health
CFDA Code
213
DUNS Number
800771594
UEI
ZUFBNVZ587D4
Project Start Date
04-September-2024
Project End Date
31-August-2025
Budget Start Date
04-September-2024
Budget End Date
31-August-2025
Project Funding Information for 2024
Total Funding
$817,483
Direct Costs
$571,773
Indirect Costs
$245,710
Year
Funding IC
FY Total Cost by IC
2024
National Institute of Neurological Disorders and Stroke
$817,483
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 1UG3AT012728-01
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
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Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
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Clinical Studies
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