CClinicalTrials.gg
TerminatedNCT03804814Updated Feb 10, 2023

Motivational Interviewing for HCV Elimination

An interventional study of Motivational Interviewing Training in Hepatitis C, sponsored by Nova Scotia Health Authority. Terminated at 1 site in Canada. Per ClinicalTrials.gov, last updated 2023-02-10.

Sponsored by Nova Scotia Health Authority · Not applicable, Interventional, and Other

Why this study was terminated
Pandemic impacted ability to recruit and enroll
Phase
Not applicable
Study type
Interventional
Enrollment
2
Allocation
Non-randomized
Sex
All
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Study summary

This study addresses a difficult barrier to hepatitis C elimination, specifically development and maintenance of a productive relationship between the health care provider and patient to ensure both treatment success and engagement in harm reduction services. Improvements in these domains may be observed through the use of a technique called "Motivational Interviewing" (MI). The aim of this study is to determine whether a customized motivational interviewing curriculum by general primary care and addictions medicine primary care providers changes rates of curative hepatitis C therapy completion.

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Conditions studied

  • Hepatitis C

Keywords

  • Motivational Interviewing
  • Healthcare delivery
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In context

Hepatitis C

2,321 studies on the registry are indexed under Hepatitis C; 102 are open to participants now.

This study's enrollment of 2 is below the median of 79 across 1,633 interventional studies indexed under Hepatitis C.

Browse Hepatitis C studies →

Lead sponsor

Nova Scotia Health Authority is the lead sponsor of 255 studies on the registry; 76 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Patient Inclusion Criteria:

  • Willingness to participate and provide informed consent
  • Positive HCV RNA Result
  • ≥18 years of age

Patient Exclusion Criteria:

  • Unwilling or unable to provide consent

Health Care Provider Inclusion Criteria:

  • Willingness to participate and provide informed consent
  • Has a hepatitis C care experience

Health Care Provider Exclusion Criteria:

  • Unwilling or unable to provide consent
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Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
2 participants (actual)

Study arms

  • Active comparator
    Motivational Interviewing Training

    Health care providers will be trained in motivational interviewing for use in Hepatitis C patient encounters.

    Behavioral: Motivational Interviewing Training

  • No intervention
    Standard Clinical Encounter

    Health care providers will not be trained in motivational interviewing for use in Hepatitis C patient encounters.

Interventions

  • BehavioralMotivational Interviewing Training

    Motivational Interviewing is a directive, client-centered counselling style intended to elicit behavior change by helping patients reach health goals through their own desires and actions. A certified and experienced Motivational Interviewing trainer will develop and deliver the curriculum to healthcare providers.

06

What researchers measure

Primary outcomes

  1. HCV Treatment Completion

    To measure the number of patients who complete HCV therapy

    Time frame: Through study completion, an average of 2 years

Secondary outcomes

  1. Time from care engagement to treatment initiation

    Time frame: Through study completion, an average of 2 years

  2. Number of unique Hepatitis C related and unrelated health system visits

    Time frame: Through study completion, an average of 2 years

  3. Number of scheduled and attended medical care appointments

    Time frame: Through study completion, an average of 2 years

  4. Self-reported intent to initiate and maintain HCV treatment assessed by questionnaire

    Time frame: Through study completion, an average of 2 years

  5. Healthcare provider knowledge, attitudes, and behavior about motivational interviewing and training assessed by questionnaire

    Time frame: Through study completion, an average of 2 years

  6. Time to complete prescribed HCV treatment course

    Time frame: Through study completion, an average of 2 years

  7. Percentage of eligible individuals that initiate HCV therapy

    Time frame: Through study completion, an average of 2 years

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Study locations

1 site
  • Nova Scotia Health Authority
    Halifax, Nova Scotia B3H 1V7, Canada
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 10, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03804814
Lead sponsor
Nova Scotia Health Authority
Responsible party
Lisa Barrett (Assistant Professor, Dalhousie University) — Principal investigator
First posted
Jan 15, 2019
Start date
May 21, 2019
Primary completion
Oct 4, 2021
Completion
Oct 4, 2021
Last update
Feb 10, 2023

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Feb 2023. You cannot join it, but the record below documents what was studied.

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