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University of Cincinnati, Swing Therapeutics study: Mobile app therapy leads to significant improvement in fibromyalgia management

July 8, 2024
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Lesley Arnold
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New research led by the University of Cincinnati and Swing Therapeutics found that a self-guided smartphone-based behavioral therapy led to significant improvements for patients with fibromyalgia.

Lesley Arnold

Credit: Photo/University of Cincinnati

New research led by the University of Cincinnati and Swing Therapeutics found that a self-guided smartphone-based behavioral therapy led to significant improvements for patients with fibromyalgia.

The multicenter, randomized controlled trial tested Stanza, a smartphone app that delivers acceptance and commitment therapy (ACT), a type of cognitive behavioral therapy recommended by international clinical guidelines for fibromyalgia management, with the results of the study published July 8 in The Lancet.

Fibromyalgia is a chronic pain condition that affects an estimated 10 million Americans, a majority of whom are women. The condition is characterized by widespread pain and other physical and cognitive symptoms that include fatigue, disrupted sleep, reduced physical function, memory problems and difficulty concentrating (“brain fog”). It is often accompanied by anxiety and depression.

The Phase 3 PROSPER-FM trial clinically validated Stanza’s benefits, including improvements in well-being, fibromyalgia severity and major fibromyalgia symptoms, including pain intensity, pain interference, fatigue, sleep disturbance, depression and physical function. This study is the largest medical device study for fibromyalgia ever undertaken.

“For the millions of people with fibromyalgia, the publication of this data in The Lancet and the clear results represent an answer to the urgent need for effective therapies to help manage their symptoms,” said Lesley Arnold, MD, study principal investigator and professor emerita at the University of Cincinnati College of Medicine. “Few large-scale studies over the last two decades have shown clinical benefit of novel treatments for this underrecognized and underserved condition.”

In the 12-week trial, 275 participants were randomized to receive either Stanza treatment or a digital symptom tracker control. At week 12, 70.6% of participants in the Stanza arm reported an improvement on Patient Global Impression in Change, which measures patient well-being.

Stanza also exhibited statistically greater improvement compared to the control on fibromyalgia-related symptoms, function and impact, as well as pain intensity, pain interference, fatigue, sleep disturbance and depression, with no treatment-related adverse events observed.

“Fibromyalgia options are typically limited to a handful of pharmacological interventions that have limited efficacy and that can come with difficult-to-manage side effects,” said Mike Rosenbluth, CEO of Swing. “This publication validates Stanza as a guideline-directed non-drug approach that many patients previously couldn’t access due to few available trained clinicians, geographic limitations and cost.



Journal

The Lancet

DOI

10.1016/S0140-6736(24)00909-7

Method of Research

Randomized controlled/clinical trial

Subject of Research

People

Article Title

Self-guided digital behavioural therapy versus active control for fibromyalgia (PROSPER-FM): a phase 3, multicentre, randomised controlled trial

Article Publication Date

8-Jul-2024

COI Statement

RMG reports being a consultant and receiving stock options or bond holdings from Swing Therapeutics. LMM reports being a consultant to Swing Therapeutics. DAW reports being a consultant to Community Health Focus and Swing Therapeutics and receiving grants from the National Institutes of Health and Patient-Centered Outcome Research Institute. YD, NV, ZG, KG, and ACK report receiving stock options and salary from Swing Therapeutics. MJR reports being a founder, chief executive officer, and receiving stock options and salary from Swing
Therapeutics. JMZ and DR report receiving grants from Swing Therapeutics (as study site investigators for the clinical investigation presented in this manuscript). DR reports salary from Bristol Myers Squibb. ALC reports being a consultant to Scilex Pharmaceuticals and Swing Therapeutics, and receiving grants from the National Institutes of Health, the US Department of Defense, and the Cystic Fibrosis Foundation. DJC reports being a consultant to AbbVie, Allergan, Aptinyx, Eli Lilly, H Lundbeck A/S, Heron Therapeutics, Neumentum, Regeneron Pharmaceuticals, Samumed, Swing Therapeutics, Tonix Pharmaceuticals, Virios Therapeutics, and serving as speaker for or receiving honoraria from Fasken Martineau DuMoulin LLP, Kellogg, Hansen, Todd, Figel & Frederick, Marks & Clerk Law, Nix Patterson, Pfizer, Zuber Lawler, and Del Duca. BV reports being an employee of Rho and a consultant to Swing Therapeutics. LMA reports being a consultant to Analgesic Solutions, Aptinyx, Axsome Therapeutics, Eliem Therapeutics, Ono Pharmaceuticals, and Scilex, and receiving grants from AbbVie, Aptinyx, Otsuka, Swing Therapeutics (principal investigator for the clinical investigation presented in this manuscript), Teva Pharmaceuticals, Tonix Pharmaceuticals, and Virios Therapeutics. JVL reports receiving a grant from Centro de Investigación Biomédica
en Red de Epidemiología y Salud Pública.

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