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Healthy Opioid Prescription Engagement (HOPE)

Primary Purpose

Opioid Misuse, Opioid-Related Disorders, Pharmacist-Patient Relations

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Patient Navigation
Standard Medication Counseling (SMC)
Sponsored by
Jerry Cochran
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Opioid Misuse focused on measuring Community Pharmacies, Patient Navigation, Opioid intervention

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adult (≥18 years)
  • English speaking
  • Not receiving cancer treatment
  • Who have a positive opioid misuse screen on the POMI will be eligible to learn about this study

Exclusion Criteria:

  • Are pregnant (given potential pre/post-natal opioid use complications among pregnant women/offspring
  • Can-not provide collateral contact information for ≥2 contact persons (to ensure consistent contact/follow up)
  • Do not have a reliable land line or mobile phone to be contacted by study staff
  • Are filling only buprenorphine (given some formulations are not indicated for pain)
  • Plan to leave the area for an extended period of time in the next 6 months
  • Have had a psychotic and/or manic episode in the last 30 days (before consent, patients will be asked to screen for psychosis
  • Do not provide permission to access their state prescription drug monitoring data.

Sites / Locations

  • University of UtahRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Brief Intervention Medication Therapy Management (BI-MTM)

Standard of Care

Arm Description

Brief Intervention Medication Therapy Management (BI-MTM) is the overarching model made up of 4 evidence-based components: Medication Therapy Management (MTM); Screening, Brief Intervention, and Referral to Treatment (SBIRT); naloxone dispensing, and Patient Navigation (PN). Each component is sequentially delivered within the model and addresses a critical aspect of opioid medication misuse and risk. The pharmacy-based portion of BI-MTM (MTM+SBIRT+naloxone) will be delivered by a PharmD level pharmacist, and PN will be delivered by a bachelor's level interventionist.

Standard of Care is the treatment as usual condition, which follows federal and Utah state pharmacy requirements for pharmacists where in patients filling prescriptions receive information and opt-in counseling. Specifically, SMC in Utah requires pharmacists to: (1) offer counseling, (2) document counseling has been offered, (3) offer a counseling process for patients not present, and (4) discuss generic substitution.The duration of SMC in the current study is a single 5-10 minute session delivered by a University of Utah pharmacist other than the study pharmacist that possesses a similar level of education and professional licensing.

Outcomes

Primary Outcome Measures

Change in opioid medication misuse.
This outcome will be assessed using the Prescription Opioid Misuse Index (POMI).

Secondary Outcome Measures

Full Information

First Posted
November 8, 2021
Last Updated
December 14, 2022
Sponsor
Jerry Cochran
Collaborators
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT05141266
Brief Title
Healthy Opioid Prescription Engagement
Acronym
HOPE
Official Title
Healthy Opioid Prescription Engagement 2.0
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
November 8, 2021 (Actual)
Primary Completion Date
January 1, 2026 (Anticipated)
Study Completion Date
December 1, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Jerry Cochran
Collaborators
National Institute on Drug Abuse (NIDA)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study is a randomized controlled trial across 14 community pharmacies to test the efficacy of the Brief Intervention-Medication Therapy Management intervention (BI-MTM). The establishment of the BI-MTM model will result in a major impact for addressing the opioid epidemic, preventing opioid use disorder and overdose, and safeguarding patient health in a novel community-based service setting.
Detailed Description
This study examines a community pharmacy-based intervention to reduce opioid medication misuse. Despite a recent national decline in opioid prescribing, 10.3 million Americans in 2018 reported misusing a prescribed opioid, and within this population, >36% of those who misused obtained the opioid medication by filling a prescription. The point of medication dispensing, namely, the community pharmacy, is an untapped resource to address prescription opioid misuse-especially when considering the >60,000 pharmacies employing >170,000 pharmacists in the US. This study aims to conduct a fully-powered RCT of the BI-MTM intervention in community pharmacy settings that will accomplish 3 Specific Aims. The first Aim will demonstrate the pharmacist-led BI-MTM intervention is superior to standard medication counseling (SMC) for mitigating opioid medication misuse. This will be accomplished by conducting a powered single-blinded randomized trial to test the efficacy of BI-MTM (n=175) vs. SMC (n=175). Participants will be screened/recruited for eligibility at point of dispensing in 14 community pharmacies in Utah, a high opioid prescribing and opioid-adverse event state. Participants will be assessed at baseline, 2, and 6 months for opioid medication misuse. Participant-level state prescription drug monitoring data will also be linked with patient outcomes to assess objective changes in medication misuse behaviors (e.g., early refills and doctor/pharmacy shopping). The second Aim will identify the pathway by which BI-MTM results in improvements for depression, pain, and subsequently opioid misuse. To accomplish this, a path analysis will assess relationships of BI-MTM: (1) on depression, pain, and misuse, (2) depression on misuse, and (3) pain on misuse. The final Aim will explore latent transitions of baseline to post-intervention misuse classes by intervention group. This will be accomplished by using mixture modeling, specifically multi-group latent transition analysis. The observed misuse indicators will be used to estimate latent class transitions across time, grouping by treatment condition and adjusting for baseline covariates. Completing SA1- 3 advance the understanding of BI-MTM efficacy and set the stage for a national multisite trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opioid Misuse, Opioid-Related Disorders, Pharmacist-Patient Relations
Keywords
Community Pharmacies, Patient Navigation, Opioid intervention

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
350 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Brief Intervention Medication Therapy Management (BI-MTM)
Arm Type
Experimental
Arm Description
Brief Intervention Medication Therapy Management (BI-MTM) is the overarching model made up of 4 evidence-based components: Medication Therapy Management (MTM); Screening, Brief Intervention, and Referral to Treatment (SBIRT); naloxone dispensing, and Patient Navigation (PN). Each component is sequentially delivered within the model and addresses a critical aspect of opioid medication misuse and risk. The pharmacy-based portion of BI-MTM (MTM+SBIRT+naloxone) will be delivered by a PharmD level pharmacist, and PN will be delivered by a bachelor's level interventionist.
Arm Title
Standard of Care
Arm Type
Other
Arm Description
Standard of Care is the treatment as usual condition, which follows federal and Utah state pharmacy requirements for pharmacists where in patients filling prescriptions receive information and opt-in counseling. Specifically, SMC in Utah requires pharmacists to: (1) offer counseling, (2) document counseling has been offered, (3) offer a counseling process for patients not present, and (4) discuss generic substitution.The duration of SMC in the current study is a single 5-10 minute session delivered by a University of Utah pharmacist other than the study pharmacist that possesses a similar level of education and professional licensing.
Intervention Type
Behavioral
Intervention Name(s)
Patient Navigation
Intervention Description
PN involves 8 weekly telephonic sessions lasting 30-45 minutes (telephonic to support lower-costs/sustainability). In session 1, the navigator reviews with the participant a report of scores from the baseline assessment to understand the participant's current health needs/challenges; session 1 also involves development of therapeutic alliance/rapport and goal setting. Sessions 2-4 focus on goal setting and identifying barriers and problem resolutions. The navigator elicits motivation and discusses this in context of readiness to change heath behavior and self-management skills. Sessions 2-4 also involve navigators supporting/assisting patients to fill out paperwork and enroll in needed social services and/or mental/behavioral/physical healthcare, including but not limited to primary care. Sessions 5-7 focus on encouraging and reinforcing treatment adherence, review-ing and identifying other care needs, and offering linkages to service providers as applicable
Intervention Type
Other
Intervention Name(s)
Standard Medication Counseling (SMC)
Intervention Description
SMC participants receive a single medication information/counseling session delivered by a University of Utah pharmacist to: (1) offer counseling, (2) document counseling was offered, (3) offer a counseling process for patients not present (not applicable to this study given all patients must screen in person), and (4) discuss generic substitution.
Primary Outcome Measure Information:
Title
Change in opioid medication misuse.
Description
This outcome will be assessed using the Prescription Opioid Misuse Index (POMI).
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult (≥18 years) English speaking Not receiving cancer treatment Who have a positive opioid misuse screen on the POMI will be eligible to learn about this study Exclusion Criteria: Are pregnant (given potential pre/post-natal opioid use complications among pregnant women/offspring Can-not provide collateral contact information for ≥2 contact persons (to ensure consistent contact/follow up) Do not have a reliable land line or mobile phone to be contacted by study staff Are filling only buprenorphine (given some formulations are not indicated for pain) Plan to leave the area for an extended period of time in the next 6 months Have had a psychotic and/or manic episode in the last 30 days (before consent, patients will be asked to screen for psychosis Do not provide permission to access their state prescription drug monitoring data.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Gerald Cochran, PhD
Phone
801/213-0799
Email
jerry.cochran@hsc.utah.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Kristi Carlston, BS
Phone
801/213-0799
Email
kristi.carlston@hsc.utah.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gerald Cochran, PhD
Organizational Affiliation
University of Utah
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Utah
City
Salt Lake City
State/Province
Utah
ZIP/Postal Code
84108
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gerald Cochran, PhD, MSW
Phone
801-213-0654
Email
jerry.cochran@hsc.utah.edu
First Name & Middle Initial & Last Name & Degree
Kristi Carlston, BS
Phone
801/213-0799
Email
kristi.carlston@utah.edu

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35417771
Citation
Cochran G, Shen J, Cox N, Field C, Carlston K, Sengpraseut B, White A, Okifuji A, Jackman C, Haaland B, Ragsdale R, Gordon AJ, Tarter R. Addressing opioid medication misuse at point of service in community pharmacy: A study protocol for an interdisciplinary behavioral health trial. Contemp Clin Trials. 2022 May;116:106759. doi: 10.1016/j.cct.2022.106759. Epub 2022 Apr 11.
Results Reference
derived

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Healthy Opioid Prescription Engagement

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