A Pilot Study of Ambulatory Heart Rate Variability Biofeedback for Substance Use Disorder

Sponsor
Massachusetts General Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05454657
Collaborator
Colorado State University (Other)
100
2
23

Study Details

Study Description

Brief Summary

Heart rate variability biofeedback (HRVB) is an biobehavioral intervention involving rhythmic breathing at resonance frequency that stimulates cardiovascular regulatory systems to help individuals better regulate affect and bolster cognitive control. This intervention has already shown its potential as a substance use disorder (SUD) treatment tool, but practical limitations of its accessibility, labor intensiveness, and cost have previously prevented this intervention from going to scale. Second-generation, ambulatory HRVB technology, however, has overcome these limitations and now allows patients to practice HRVB in-the-moment when its needed most. This study is testing the efficacy of second-generation, ambulatory HRVB for the first time with individuals with SUD.

Condition or Disease Intervention/Treatment Phase
  • Device: Heart rate variability biofeedback + treatment as usual
  • Behavioral: Treatment as usual only
N/A

Detailed Description

Alcohol and other drug use (AOD) lapses in early substance use disorder (SUD) recovery typically arise from interactions between aversive affective states and stressors that together elicit urges to use. A central goal of first-line cognitive-behavioral SUD treatments is to strengthen affective and cognitive control to increase individuals' ability to override impulses to use AOD. Yet certain automatic physiological processes compromised by SUD dynamically interact with internal affective states and environmental cues to undermine effortful cognitive control and outcompete cognitive goals to avoid substance use.

Heart rate variability biofeedback (HRVB) is a biobehavioral intervention involving rhythmic breathing at resonance frequency (RF) that stimulates the body's baroreflex mechanism to offset these psychophysiological deficits. The autonomic normalization effected by RF breathing is thought to bolster cognitive control efforts by interrupting or dampening automatic-visceral reactions that can undermine treatment gains, and in doing so support better decision-making, motivation, reductions in craving, and shifts in attention allocation.

Previous studies of HRVB have focused on positive behavioral effects that accrue over a series of weeks or months, rather than 'in-the-moment'. These chronic behavior changes, although clinically valuable, are labor and time intensive to elicit, reducing the likelihood of large-scale uptake of the intervention. Further, first-generation HRVB's regular daily practice model is likely to only partially mitigate the intense momentary bouts of emotion dysregulation that are triggers for AOD use in those in early SUD recovery. In contrast, recent studies have demonstrated that a brief exposure to RF breathing in anticipation of psychosocial stress, or during induced stress, helps to control physiological arousal, reduce state anxiety, and improve cognitive performance. It is posited that such bursts of in-the-moment HRVB practice could serve as a potent SUD treatment tool that helps individuals self-regulate emotions when needed most.

Recent advances in the field have given rise to small, lightweight, wearable biosensors that can allow wearers to do HRVB on-the-go. These devices also have the capacity to function as a just-in-time intervention by prompting in-the-moment HRVB practice when autonomic hyperarousal is detected, to buffer salient triggers and urges to use AOD. This research builds on a body of preliminary work speaking to HRVB's potential as an addendum to first-line SUD treatments by exploring for the first time in this disorder this second-generation, ambulatory, HRVB technology. Specific aims of this research include, 1) assessing ambulatory HRVB's uptake by individuals with SUD, 2) testing day-level effects of in-the-moment HRVB practice on affective states and substance use, and 3) testing the accumulative effects of scheduled daily HRVB practice, in-the-moment HRVB practice, and their interaction, on substance use.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Heart rate variability biofeedback + treatment as usual vs. treatment as usual onlyHeart rate variability biofeedback + treatment as usual vs. treatment as usual only
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Pilot Study of Ambulatory Heart Rate Variability Biofeedback for Substance Use Disorder
Anticipated Study Start Date :
Aug 1, 2022
Anticipated Primary Completion Date :
Jul 1, 2024
Anticipated Study Completion Date :
Jul 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Heart rate variability biofeedback + treatment as usual

The experimental group will participate in 8 weeks of heart rate variability biofeedback practice using the Lief heart rate variability biofeedback Smart Patch and smartphone app + treatment as usual. Participants will be asked to, 1) wear the Lief Smart Patch for at least 6 hours per day, 2) do 10mins of scheduled heart rate variability biofeedback practice twice daily, and 3) use it as needed in response to negative affect in-the-moment.

Device: Heart rate variability biofeedback + treatment as usual
Heart rate variability biofeedback is a biobehavioral intervention involving rhythmic breathing at resonance frequency (RF) that stimulates the baroreflex and increases heart rate variability. Treatment as usual may include any outpatient substance use disorder treatment or mutual-help group participation.

Behavioral: Treatment as usual only
Treatment as usual may include any outpatient substance use disorder treatment or mutual-help group participation.

Active Comparator: Treatment as usual only

The control group will participate in 8 weeks of treatment as usual only.

Behavioral: Treatment as usual only
Treatment as usual may include any outpatient substance use disorder treatment or mutual-help group participation.

Outcome Measures

Primary Outcome Measures

  1. Heart rate variability biofeedback engagement [8 weeks]

    Heart rate variability biofeedback (HRVB) engagement reflected by HRVB practice time. As a general benchmark of intervention uptake success, we will accept ≥50% engagement/adherence to scheduled practice (i.e., 10mins, twice daily) with consideration given to both number of days practiced and time practiced each day. We will also accept ≥50% in-the-moment practice as indicative of engagement/adherence, based on the ratio of just-in-time practice prompts responded to vs. ignored and the number of days participants engaged in in-the-moment HRVB practice.

  2. Day-level substance use [8 weeks]

    Day-level substance use measured by ecological momentary assessment

  3. Day-level negative affect [8 weeks]

    Day-level negative affect measured by ecological momentary assessment

  4. Day-level craving [8 weeks]

    Day-level craving measured by ecological momentary assessment

  5. Day-level positive affect [8 weeks]

    Day-level positive affect measured by ecological momentary assessment

  6. 8-week substance use [8 weeks]

    Substance use over the 8-week intervention period expressed as percent days abstinent measured by ecological momentary assessment

  7. Change negative affect [8 weeks]

    Change in negative affect measured by ecological momentary assessment over the 8-week intervention period, modeled using time-varying effects modeling (TVEM).

  8. Change craving [8 weeks]

    Change in craving measured by ecological momentary assessment over the 8-week intervention period, modeled using time-varying effects modeling (TVEM).

  9. Change positive affect [8 weeks]

    Change in positive affect measured by ecological momentary assessment over the 8-week intervention period, modeled using time-varying effects modeling (TVEM).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • ≥18 years of age

  • Own a smartphone

  • English proficiency

  • DSM 5 diagnosis of substance use disorder

  • In the first year of a current substance use disorder recovery attempt with a goal of total alcohol and other drug abstinence

  • Current engagement in outpatient addiction treatment or mutual-help

Exclusion Criteria:
  • Medical history of severe cardiac arrhythmia

  • Active psychosis

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Massachusetts General Hospital
  • Colorado State University

Investigators

  • Principal Investigator: David Eddie, Ph.D., Massachusetts General Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
David Eddie, Assistant Professor, Massachusetts General Hospital
ClinicalTrials.gov Identifier:
NCT05454657
Other Study ID Numbers:
  • 2022P001496
First Posted:
Jul 12, 2022
Last Update Posted:
Jul 12, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by David Eddie, Assistant Professor, Massachusetts General Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 12, 2022