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Completed Phase 3 Interventional

Prospective Study to Evaluate a Digital Regimen for Fibromyalgia Management

ClinicalTrials.gov ID: NCT05243511

Public ClinicalTrials.gov record NCT05243511. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 8:47 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

"PROSPER-FM": Prospective Study to Evaluate a Digital Regimen for Fibromyalgia Management

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

PROSPER-FM is a multi-center, randomized, non-significant risk device study to evaluate the safety and efficacy of two digital therapy smartphone applications in participants with fibromyalgia. Eligible participants are randomized (1:1) to either the Digital Acceptance and Commitment Therapy (Digital ACT) group or the Digital Symptom Tracker group and receive assigned therapy for 12 weeks.

Study identification

NCT ID
NCT05243511
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Swing Therapeutics, Inc.
Other
Enrollment
275 participants

Conditions and interventions

Conditions

Interventions

Device · Other

Eligibility (public fields only)

Age range
22 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 8, 2022 (Actual)
Primary completion
May 15, 2023 (Actual)
Completion
May 15, 2023 (Actual)
Last update posted
Jun 15, 2023

2022 – 2023

United States locations

U.S. sites
25
U.S. states
12
U.S. cities
25
Facility City State ZIP Site status
Site #37 Covina California 91722 —
Site #15 Oceanside California 92056 —
Site #31 San Bernardino California 92498 —
Site #38 Thousand Oaks California 91360 —
Site #36 Tujunga California 91042 —
Site #35 Whittier California 90602 —
Site #13 Orlando Florida 32801 —
Site #33 St. Petersburg Florida 33709 —
Site #25 Atlanta Georgia 30329 —
Site #21 Covington Louisiana 70433 —
Site #20 New Orleans Louisiana 70124 —
Site #22 Prairieville Louisiana 70769 —
Site #39 Chestnut Hill Massachusetts 02467 —
Site #24 Ocean Springs Mississippi 39564 —
Site #34 Brooklyn New York 11235 —
Site #32 Scarsdale New York 10583 —
Site #12 Williamsville New York 14221 —
Site #27 Fargo North Dakota 58104 —
Site #14 Cincinnati Ohio 45219 —
Site #28 Dayton Ohio 45419 —
Site #23 Tulsa Oklahoma 74133 —
Site #16 Allentown Pennsylvania 18104 —
Site #29 Austin Texas 78726 —
Site #26 McKinney Texas 75070 —
Site #30 Pflugerville Texas 78660 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05243511, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 15, 2023 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05243511 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →