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Reducing Sedentary Time in Fibromyalgia Patients (ReSeT-FM)

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Indiana University

Status

Completed

Conditions

Fibromyalgia
Veterans

Treatments

Behavioral: ReSeT-FM intervention

Study type

Observational

Funder types

Other
Other U.S. Federal agency

Identifiers

NCT03247348
1702201230

Details and patient eligibility

About

This study evaluates the feasibility of a behavioral intervention designed to replace sedentary behavior with light physical activity in veterans with Fibromyalgia. The study will also evaluate the acceptability of the intervention among veterans and intervention effects on pain and physical function.

Full description

Recent research suggests that individuals with Fibromyalgia (FM) who spend more time in sedentary behavior and less time in light physical activity experience greater clinical pain and overall impact of FM, irrespective of time spent in moderate to vigorous physical activity. To date, no studies have investigated the potential impact of reducing sedentary behavior on key clinical and physical function outcomes in FM. The overall objective of the pilot project is to design and evaluate the feasibility of an 8-week behavioral intervention designed to replace sedentary behavior with light physical activity in veterans with FM. Mixed (quantitative and qualitative) methods will be used to evaluate the behavioral intervention, which is based on constructs from social cognitive and self-regulatory theories that consistently identify important drivers of behavior change as: education, goal-setting, self-monitoring and behavioral prompts to move via an activity tracker and phone app, and feedback on behavior via weekly meetings.

Enrollment

10 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Veterans will be eligible if they have:

  • 2010 American College of Rheumatology (ACR) diagnostic criteria for fibromyalgia: Widespread Pain Index (WPI) greater than 7 and Symptom Severity Scale (SS) greater than 5 or WPI 3-6 and SS greater than 9.
  • Symptoms have been present at a similar level for at least 3 months
  • The subject does not have a disorder that would otherwise explain the pain
  • Moderate pain severity (pain severity score greater than 5)
  • No changes in fibromyalgia medications for last 4 weeks
  • Self-reporting at least 8 hours per day sitting on 5 or more days per week
  • Having access to either an Android or iPhone smart phone with access to internet

Exclusion criteria

  • Significant cardiovascular disease
  • chronic obstructive pulmonary disease (COPD) or asthma needing home oxygen
  • Stroke or transient ischemic attack (TIA) in last 6 months
  • Cancer (other than skin cancer) and receiving treatment for it
  • Active psychosis
  • Active suicidal ideation
  • Moderate to severe cognitive impairment
  • Engaging in more than 30 minutes of moderate to vigorous physical activity 3 or more days per week
  • Currently using an app or activity tracker to track physical activity
  • Enrolled in another research study related to pain or exercise

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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