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Combined Guanfacine and Mindfulness Meditation As an Adjunct to Buprenorphine Maintenance in Opioid Use Disorder

Phase 1
Not yet recruiting
Conditions
Mindfulness
Guanfacine
Opioid Use Disorder
Interventions
Behavioral: Mindfulness Oriented Recovery Enhancement (MORE)
Registration Number
NCT06642181
Lead Sponsor
Rutgers, The State University of New Jersey
Brief Summary

The US is currently going through an opioid crisis, and while Medication Assisted Treatments such as buprenorphine (BUP) have proved highly effective at stabilizing the neurobiology underlying acute withdrawal, they have been less effective at preventing longer-term relapse and adherence. This may be due to the fact that they do not fully engage the neural processes sub-serving the emotional control of sensitized negative mood and reward sensitivity during stress- and opioid-cue provocation, respectively. In contrast while the alpha2 agonist, guanfacine, may attenuate stress-provoked opioid craving by mediating top-down prefrontal control over sensitized dysphoria, the behavioral intervention, Mindfulness Oriented Recovery Enhancement (MORE) may reduce opioid cue-provoked craving by mediating top-down prefrontal control over hedonic dysregulation. Furthermore, while both interventions separately may prove effective as longer-term adjunctive therapies, they may offer greater efficacy together, providing a unique medication/behavioral combination able to target both stress and reward provocation mechanisms. To optimally test this hypothesis, a staged approach is proposed to first confirm the efficacy of both GXR and MORE, independently and combined (R61), prior to elucidating underlying neural mechanisms (R33). Using a 2 X 2 design, N=80 OUD individuals on BUP will be randomized to either 6-weeks of Guanfacine extended release (GXR; 3mgs, n=40) or placebo (PBO; n=40). Half of all participants in each group will then receive either weekly MORE, or a Support Group (SG) control, creating four intervention groups (Control Grp: PBO+SG, n=20); (GXR Grp: GXR+SG, n=20); (MORE Grp: PBO+ MORE, n=20); (Combined Grp: GXR+MORE, n=20). A pre- and post-laboratory study will be conducted before and after six weeks of intervention where participants will be randomly exposed to 3 personalized guided imageries (stress, opioid cue, neutral). Subjective measures of opioid craving, anxiety, mood, stress, emotional reappraisal, and heart rate will be collected before and after imagery exposure. Following milestone completion, an identical design is proposed in N=144 individuals, where participants will be exposed to imageries in the MRI scanner (R33). On the basis of prior research, it is hypothesized in that GXR will attenuate opioid craving and improve emotion regulation during stress, while MORE will demonstrate the same effects during opioid cue exposure. Combined GXR and MORE will also demonstrate additive or synergistic improvements compared with each intervention alone (R61). The effects of GXR on opioid cue- and MORE on stress-provoked opioid seeking will be explored. In the R33 component, it is hypothesized that GXR will improve regulatory and affective brain function during stress, and MORE will improve regulatory and reward function during opioid cue exposure. Combined GXR and MORE may improve regulatory function in an additive or synergistic manner (R33). Findings will help elucidate the efficacy and neural mechanisms underpinning a novel integrated pharmaco-behavioral therapy for OUD individuals maintained on BUP.

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
224
Inclusion Criteria

N=224 individuals with a history of SCID-5 OUD, and maintained on BUP for at least 4 weeks (N=80 in the R61 phase and N=144 in the R33 phase). These individuals must be:

  • aged 18 to 55 years and have a body mass index (BMI) of 18-35;
  • have a positive urine toxicology screen for non-prescription opioids
  • be in good health as verified by screening examination
  • able to read English and provide informed consent.
Exclusion Criteria
  • Current SCID V criteria for a moderate to severe substance use disorder other than opioids or nicotine (although mild use will be permitted)
  • Use of medications in the last 6 months that may affect cerebral function with the exception of BUP and individuals stabilized on SSRIs
  • psychotic or severely psychiatrically disabled (i.e. suicidal, current mania)
  • hypotensive individuals with sitting blood pressure below 100/50 mmHG
  • Women who are pregnant, nursing or refuse to use a reliable form of birth control
  • EKG evidence at baseline screening of any clinically significant conduction abnormalities (Bazett's QTc of >450 msec for men and QTc>470 msec for women)
  • R33 phase will additionally include failure to satisfy fMRI safety protocols.

Study & Design

Study Type
INTERVENTIONAL
Study Design
FACTORIAL
Arm && Interventions
GroupInterventionDescription
Combined GroupGuanfacine pharmacotherapyWill receive both Guanfacine pharmacotherapy and MORE intervention
MORE GroupMindfulness Oriented Recovery Enhancement (MORE)Will receive MORE intervention and placebo medication
Guanfacine GroupGuanfacine pharmacotherapyWill receive Guanfacine intervention and Support group control (non-mindfulness) intervention
Combined GroupMindfulness Oriented Recovery Enhancement (MORE)Will receive both Guanfacine pharmacotherapy and MORE intervention
Primary Outcome Measures
NameTimeMethod
AnxietyAt pre- and post-intervention (6 weeks intervention)

Self report of anxiety will be collected. Will be measured using a likert scale 0 (not at all) to 10 (extreme). .

StressAt pre- and post-intervention (6 weeks intervention)

Self report of stress will be collected. Will be measured using a likert scale 0 (not at all) to 10 (extreme).

MoodAt pre- and post-intervention (6 weeks intervention)

Self report of mood will be collected. Positive and negative mood will be collected on a 4 point likert scale 0 (not at all) and 4 (extreme)

Emotional DysregulationAt pre- and post-intervention (6 weeks intervention)

Self report of emotional dysregulation data will be collected. Will be measured using a 10 point likert scale (0=not at all) and 10 (extreme)

Heart RateAt pre- and post-intervention (6 weeks intervention)

Heart rate data will be collected using an EKG monitor during the entire lab procedure while the participants will hear stress, opioid, and neutral related scripts.

CravingAt pre- and post-intervention (6 weeks intervention)

Self report of opioid craving will be collected. Will be measured using a likert scale 0 (not at all) to 10 (extreme).

Brain ActivationAt pre- and post-intervention (6 weeks intervention)

Brain activation data will be collected using Blood Oxygen Level Dependent (BOLD) signal during functional magnetic resonance imaging (fMRI) while participants hear stress, opioid and neutral scripts.

Brain ConnectivityAt pre- and post-intervention (6 weeks intervention)

Brain connectivity data will be collected using Blood Oxygen Level Dependent (BOLD) signal during functional magnetic resonance imaging (fMRI) while participants hear stress, opioid and neutral scripts.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Rutgers School of Health Professions

🇺🇸

Newark, New Jersey, United States

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