NCT00643435

Brief Summary

Patient self-efficacy, or confidence in one's ability to take the necessary steps to achieve a goal, has been shown to influence a number of important health behaviors and outcomes. However, current ways of increasing patient self-efficacy are time and labor intensive and occur away from doctor visits, where most health care is delivered. We developed, and are testing in a study the effectiveness of a new way of teaching doctors how to talk to patients during office visits in a way that will boost their patients' self-efficacy for changing important health behaviors.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
64

participants targeted

Target at P25-P50 for not_applicable diabetes

Timeline
Completed

Started Feb 2006

Typical duration for not_applicable diabetes

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2006

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2007

Completed
9 months until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2008

Completed
23 days until next milestone

First Submitted

Initial submission to the registry

March 24, 2008

Completed
2 days until next milestone

First Posted

Study publicly available on registry

March 26, 2008

Completed
Last Updated

March 26, 2008

Status Verified

March 1, 2008

Enrollment Period

1.3 years

First QC Date

March 24, 2008

Last Update Submit

March 25, 2008

Conditions

Keywords

self-efficacychronic illnesshealth behavioreducation, medical, residency

Outcome Measures

Primary Outcomes (1)

  • Resident physician use of self-efficacy enhancing patient interviewing techniques, assessment via coding of audio recordings from standardized patient encounters

    Within 6 months of completion of intervention

Study Arms (2)

1

EXPERIMENTAL

These residents receive training provided by standardized patient instructors, in use of self-efficacy enhancing interviewing techniques to support patient health behavior change,

Behavioral: Self-efficacy enhancing interviewing techniques training

2

ACTIVE COMPARATOR

These residents receive training provided by a standardized patient instructor, regarding the common co-occurrence of chronic medical and mental health problems, without any interviewing technique discussion or training.

Behavioral: Control intervention

Interventions

Teaching by standardized patient instructors regarding use of self-efficacy enhancing interviewing techniques to be applied in patient encounters

1

These residents receive training provided by a standardized patient instructor, regarding the common co-occurrence of chronic medical and mental health problems, without any interviewing technique discussion or training.

2

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Family medicine or internal medicine residents in training at the University of California Davis Medical Center

You may not qualify if:

  • None

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Diabetes MellitusDepressionAnxiety DisordersAsthmaStress Disorders, Post-TraumaticChronic DiseaseHealth Behavior

Condition Hierarchy (Ancestors)

Glucose Metabolism DisordersMetabolic DiseasesNutritional and Metabolic DiseasesEndocrine System DiseasesBehavioral SymptomsBehaviorMental DisordersBronchial DiseasesRespiratory Tract DiseasesLung Diseases, ObstructiveLung DiseasesRespiratory HypersensitivityHypersensitivity, ImmediateHypersensitivityImmune System DiseasesStress Disorders, TraumaticTrauma and Stressor Related DisordersDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Anthony F Jerant, MD

    Department of Family and Community Medicine, University of California Davis School of Medicine

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER

Study Record Dates

First Submitted

March 24, 2008

First Posted

March 26, 2008

Study Start

February 1, 2006

Primary Completion

June 1, 2007

Study Completion

March 1, 2008

Last Updated

March 26, 2008

Record last verified: 2008-03