Sleep and Pain Interventions in Women With Fibromyalgia

Description

Insomnia affects 67-88% of chronic pain patients. SPIN II is a randomized controlled clinical trial that will compare the effects of two cognitive behavioral sleep treatments in women with fibromyalgia and insomnia. This trial will yield important information about the roles of sleep, arousal, and brain structure and function in the development and maintenance of chronic pain in women with fibromyalgia.

Conditions

Fibromyalgia, Insomnia, Chronic Widespread Pain

Study Overview

Study Details

Study overview

Insomnia affects 67-88% of chronic pain patients. SPIN II is a randomized controlled clinical trial that will compare the effects of two cognitive behavioral sleep treatments in women with fibromyalgia and insomnia. This trial will yield important information about the roles of sleep, arousal, and brain structure and function in the development and maintenance of chronic pain in women with fibromyalgia.

Impact of CBT for Insomnia on Pain Symptoms and Central Sensitization in Fibromyalgia

Sleep and Pain Interventions in Women With Fibromyalgia

Condition
Fibromyalgia
Intervention / Treatment

-

Contacts and Locations

Columbia

University of Missouri- Department of Psychiatry, Columbia, Missouri, United States, 65210

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * female
  • * 18+ years of age
  • * willing to be randomized
  • * can read and understand English
  • * diagnosed with Fibromyalgia and insomnia
  • * no prescript or over the counter pain or sleep medicaments for 1+ month
  • * unable to provide informed consent
  • * cognitive impairment
  • * sleep disorder other than insomnia (i.e., sleep apnea, periodic limb movement disorder
  • * bipolar or seizure disorder
  • * other major psychopathology (other than depression or anxiety)
  • * psychotropic or other medications that alter pain or sleep
  • * participation in non-pharmacological treatment (including CBT) for pain, sleep, or mood outside current trial
  • * internal metal objects or electrical devices
  • * pregnancy

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

FEMALE

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Missouri-Columbia,

Christina McCrae, PhD, PRINCIPAL_INVESTIGATOR, University of Missouri-Columbia

Study Record Dates

2025-05-31