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HRV Biofeedback in Pain Patients

CompletedNot applicableNCT02426476
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

Pain initiates a stress response that increases sympathetic output and leads to autonomic imbalance. Heart rate variability (HRV) is a easy to perform, valid measure of autonomic function. HRV biofeedback (HRV-B) is a novel biobehavioral procedure in which patients learn to restore autonomic balance by developing 'HRV Coherence'. Patients in HRV Coherence have improved mood and cognition. The investigators' pilot study showed that HRV-B alleviated chronic pain and stress among Veteran Pain Clinic patients. HRV-B thus has a pivotal role in managing pain. The proposed project is a randomized, sham-controlled, biobehavioral intervention with HRV-B to test the hypotheses that HRV-B increases HRV coherence and reduces pain, stress, fatigue, insomnia and depression and improves sleep, activity, and cognition in Veterans with chronic neuromuscular pain. The investigators hypothesize that HRV-B will (1) reduce self-reported pain and stress ratings, (2) improve objective measures of actigraphic sleep parameters (sleep latency, duration, efficiency, fragmentation), rest/activity rhythms (dichotomy index, interdaily stability) and cognitive function (reaction time, attention); and (3) alleviate self-reported fatigue and depression symptoms. Patients from two groups will be randomized to the investigators' previously established HRV-B or sham protocol (n=40 each), and will complete a baseline assessment, 6 weekly training sessions, a post-training assessment, and 4-week and 8-week follow-up evaluations post-training. Portable, hand-held, data-logging devices will be used to practice attaining HRV coherence at home by the active HRV-B training group, while those in the sham training group will get a 'stress squeeze ball'. Standard methods will quantify HRV coherence and other HRV measures, and validated instruments will be used to assess pain, stress, fatigue, insomnia, depression, and cognitive function. Wrist actigraphy will be used to objectively characterize insomnia via con…

Study details

Official title
HRV Biofeedback in Pain Patients: Pilot Intervention for Pain, Fatigue & Sleep
Conditions
  • Chronic Neuromuscular Pain
Interventions
  • Behavioral: active heart rate variability biofeedback training
  • Behavioral: sham HRVB training
Sponsor
VA Office of Research and Development
Collaborators
University of South Carolina
Start date
2015-06-10
Primary completion
2020-09-30
Sex
All
Results posted
Yes, on ClinicalTrials.gov
Countries
United States
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * are a Veteran between age 18 or older * have chronic, non-malignant, neuro-musculoskeletal pain Exclusion Criteria: * a history of arrhythmia requiring medication or hospitalization * a pacemaker or automatic implantable cardioverter-defibrillator * a history of ischemic heart disease, heart transplant, cardiovascular surgery within 1 year * congestive heart failure * uncontrolled hypertension * an active prescription for certain heart medications * a history of seizures or use of antiseizure or anticonvulsant medication * moderate or severe head injury or stroke * evidence of active substance abuse or dependence (alcohol or tobacco use is not be an exclusion, participants will be asked to provide information about these behaviors in the investigators' questionnaire) * a history of bipolar, psychotic, panic or obsessive-compulsive disorder (note: depression is an exclusion) * cognitive impairment (dementia), neurocognitive deficits, or a central nervous system or neurological disorder (e.g., Gulf War Syndrome) * a current or pending worker compensation claim or personal injury litigation related to the participants' symptoms

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT02426476