ClinicalTrials.gg
Enrolling by invitationNCT07814521Updated Sep 11, 2026

Clinician Motivational Interviewing Training Evaluation

An interventional study of MI training in Behavior Change Interventions, Evaluation and Training Effectiveness, sponsored by Geisinger Clinic. Enrolling by invitation at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-11.

Primary conditionCommunicationRegistry: BehaviorReclassifiedWhy we changed it
Registry
Behavior — the first condition term the registry derived for this study.
ClinicalTrials.gg
Communication
Why
  1. The study's listed conditions name Communication, a narrower term within Behavior.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Geisinger Clinic · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
180,000
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The goal of this study is to evaluate the impact of motivational interviewing (MI) training for Geisinger clinicians on their patients' health outcomes. Clinicians will be randomly assigned to attend or not attend mandated MI training, which will be provided at one of several sessions offered beginning in August 2026. Randomization will be stratified by department to ensure participant balance and that participating departments maintain necessary staffing levels during the training period. The study will assess whether there is a significant increase in patients' positive health behaviors and outcomes, as reflected in an index measure of multiple outcomes that may reasonably be facilitated by MI training: vaccinations and health screenings as reflected in electronic health record care gaps. Smoking cessation and other lifestyle modifications, preventive medication adherence, and behavioral health use may also be examined as part of an overall measure of MI impact. For each clinician assigned to the study, all patients they see in the 90-day period following the (would-be) date of that clinician's training will be identified and enrolled in the study. Outcome timeframes will then be relative to each unique patient's first encounter following (would-be) training.

02

Conditions studied

  • Behavior Change Interventions
  • Evaluation
  • Training Effectiveness
  • Health Services Research
  • Healthcare Provider Training
  • Patient-provider Communication

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Keywords

  • Behavior change interventions
  • Evaluation
  • Training effectiveness
  • Health services research
  • Healthcare provider training
  • Patient-provider communication
  • Motivational interviewing
03

In context

Communication Reclassified

719 studies on the registry are indexed under Communication; 159 are open to participants now.

This study's planned enrollment of 180,000 is above the median of 144 across 571 interventional studies indexed under Communication.

Browse Communication studies →

Lead sponsor

Geisinger Clinic is the lead sponsor of 127 studies on the registry; 17 are open to participants now.

Of its 9 completed or terminated interventional studies of FDA-regulated products, 7 (78%) have results posted.

Compared within Communication, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Behavior. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Clinician Inclusion Criteria:

  • Employed by Geisinger throughout study period
  • Working in the Community Medical Service Line (CMSL) or 65 Forward
  • MD, DO, PA

Patient Inclusion Criteria:

  • >= 18 years of age
  • Attended a CMSL or 65 Forward encounter with an enrolled clinician at least once during the study period, following the MI training

Exclusion Criteria:

  • N/A
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
180,000 participants (estimated)

Study arms

  • Experimental
    MI training

    Clinician is assigned to attend an MI training session

    Behavioral: MI training

  • No intervention
    Control

    Clinician is not assigned to MI training

Interventions

  • BehavioralMI training

    Clinicians will be instructed to register for one MI training session that will be conducted live and in person, with possible virtual training available for those unable to attend in person

06

What researchers measure

Primary outcomes

  1. Proportion of care gaps addressed

    Proportion of open care gaps closed

    Time frame: Within 180 days following initial patient encounter, as of day following (would-be) assigned MI training session

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Aug 2026 (actual). Primary completion is estimated for Aug 2028, 24 months after the start.

Of 390 non-industry interventional studies with no phase under Communication, half reached primary completion within 18 months of starting (the median), counting those still running; a quarter within 6 and three quarters within 36. This study's planned 24 months is above that.

Counting every sponsor, half of 394 studies reached it within 18 months; a quarter within 6 and three quarters within 36.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 17, 2026
First posted
Sep 11, 2026
StartActual
Aug 18, 2026
Primary completionEst.
Aug 2028
CompletionEst.
Aug 2028
Last update
Sep 11, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 11, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07814521
Lead sponsor
Geisinger Clinic
Responsible party
Amir Goren (Director, Geisinger Program Evaluation, Geisinger Clinic) — Principal investigator
First posted
Sep 11, 2026
Start date
Aug 18, 2026
Primary completion
Aug 2028 (estimated)
Completion
Aug 2028 (estimated)
Last update
Sep 11, 2026

Study contacts

Amir Goren, PhD
principal investigator · Geisinger Clinic

Oversight

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

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