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

被引:10
作者
Gendreau, R. Michael [1 ]
McCracken, Lance M. [2 ]
Williams, David A. [3 ]
Luciano, Juan, V [4 ,5 ,6 ]
Dai, Yifei [7 ]
Vega, Nicolette [7 ]
Ghalib, Zunera [7 ]
Guthrie, Kristen [7 ]
Kraus, Allison C. [7 ]
Rosenbluth, Michael J. [7 ]
Vaughn, Ben [8 ]
Zomnir, Jennifer M. [9 ]
Reddy, Dana [10 ]
Chadwick, Andrea L. [11 ]
Clauw, Daniel J. [3 ]
Arnold, Lesley M. [12 ]
机构
[1] Gendreau Consulting, Poway, CA USA
[2] Uppsala Univ, Dept Psychol, Uppsala, Sweden
[3] Univ Michigan, Chron Pain & Fatigue Res Ctr, Dept Anesthesiol, Ann Arbor, MI USA
[4] Univ Autonoma Barcelona, Dept Clin & Hlth Psychol, Barcelona, Spain
[5] Parc Sanitari St Joan de Deu, Teaching Res & Innovat Unit, St Boi De Llobregat, Spain
[6] CIBER Epidemiol & Publ Hlth, Madrid, Spain
[7] Swing Therapeut, San Francisco, CA USA
[8] Rho, Durham, NC USA
[9] DelRicht Res, Mckinney, TX USA
[10] Curavit, Scarsdale, NY USA
[11] Univ Kansas, Dept Anesthesiol Pain & Perioperat Med, Sch Med, Kansas City, KS USA
[12] Univ Cincinnati, Dept Psychiat & Behav Neurosci, Cincinnati, OH 45219 USA
关键词
COMMITMENT THERAPY; CHRONIC PAIN; ACCEPTANCE; INTERVENTION; GUIDELINES; MANAGEMENT; DIAGNOSIS;
D O I
10.1016/S0140-6736(24)00909-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background International guidelines have recommended cognitive behavioural therapy, including acceptance and commitment therapy (ACT), as it offers validated benefits for managing fibromyalgia; however, it is inaccessible to most patients. We aimed to evaluate the effect of a 12-week, self-guided, smartphone-delivered digital ACT programme on fibromyalgia management. Methods In the PROSPER-FM randomised clinical trial conducted at 25 US community sites, adult participants aged 22-75 years with fibromyalgia were recruited and randomly assigned (1:1) to the digital ACT group or an active control group that offered daily symptom tracking and monitoring and access to health-related and fibromyalgiarelated educational materials. Randomisation was done with a web-based system in permuted blocks of four at the site level. We used a blind-to-hypothesis approach in which participants were informed they would be randomly assigned to one of two potentially effective therapies under evaluation. Research staff were not masked to group allocation, with the exception of a masked statistics group while preparing statistical programming for the interim analysis. The primary endpoint was patient global impression of change (PGIC) response rate at week 12. Analyses were by intention to treat. The trial was registered with ClinicalTrials.gov, NCT05243511 (now fully closed). Findings Between Feb 8, 2022, and Feb 2, 2023, 590 individuals were screened, of whom 275 (257 women and 18 men) were randomly assigned to the digital ACT group (n=140) and the active control group (n=135). At 12 weeks, 99 (71%) of 140 ACT participants reported improvement on PGIC versus 30 (22%) of 135 active control participants, corresponding to a difference in proportions of 48<middle dot>4% (95% CI 37<middle dot>9-58<middle dot>9; p<0<middle dot>0001). No device-related safety events were reported. Interpretation Digital ACT was safe and efficacious compared with digital symptom tracking in managing fibromyalgia in adult patients. Copyright (c) 2024 Elsevier Ltd. All rights reserved, including those for text and data mining, AI training, and similar technologies.
引用
收藏
页码:364 / 374
页数:11
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