Pia Roman

Pia Roman

Auto-generated profile, based on publicly available information

Pia Roman

VA Ann Arbor Healthcare System, Center for Clinical Management Research, Ann Arbor, MI, USA

Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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8 August 2016 in Journal of Medical Internet Research
Verified
Journal Article
Open access
MMMarilyn L. Moy
Marilyn L. Moy
CMCarlos H Martinez
Carlos H Martinez
RKReema Kadri
Reema Kadri
PRPia Roman
Pia Roman
RHRobert G Holleman
Robert G Holleman
CRCaroline R Richardson
Caroline R Richardson
Journal of Medical Internet Research - International Scientific Journal for Medical Research, Information and Communication on the Internet

17 May 2023 in Contemporary Clinical Trials
Verified
Journal Article
Open access
SMSusan L. Murphy
Susan L. Murphy
SZSuzanna M. Zick
Suzanna M. Zick
RHRichard Harris
Richard Harris
SSShawna N. Smith
Shawna N. Smith
ASAnanda Sen
Ananda Sen
SKSarah L. Krein
Sarah L. Krein
Chronic low back pain is prevalent and disabling in Veterans, but effective pain management is challenging. Clinical practice guidelines emphasize multimodal pain management including evidence-based complementary and integrative health treatments such as acupressure as a first line of care. Unfortunately, the ability to replicate interventions, cost, resources, and limited access are implementation barriers. Self-administered acupressure has shown positive effects on pain and can be practiced anywhere with little to no side effects. The aims of this Type 1 hybrid effectiveness implementation randomized controlled trial are 1) to determine effectiveness of a self-administered acupressure protocol at improving pain interference and secondary outcomes of fatigue, sleep quality, and disability in 300 Veterans with chronic low back pain, and 2) evaluate implementation barriers and facilitators to scale-up acupressure utilization within Veterans Health Administration (VHA). Participants randomized to the intervention will receive instruction on acupressure application using an app that facilitates daily practice for 6 weeks. During weeks 6 through 10, participants will discontinue acupressure to determine sustainability of effects. Participants randomized to waitlist control will continue their usual care for pain management and receive study materials at the end of the study period. Outcomes will be collected at baseline and at 6- and 10-weeks post baseline. The primary outcome is pain interference, measured by the PROMIS pain interference scale. Using established frameworks and a mixed methods approach, we will evaluate intervention implementation. If acupressure is effective, we will tailor strategies to support implementation in the VHA based on study findings. NCT05423145.