Mode
Text Size
Log in / Sign up
N/A N=117 Randomized Prevention

Interprofessional Training to Improve Diabetes Care: The ReSPECT Trial

Diabetes Mellitus

Enrolled (actual)
117
Serious AEs
0.0%
Results posted
Oct 2015
Primary outcome: Primary: Provider Abilities Scale - Subscale From the Midwest (MW) Clinicians' Network — 6.89; 6.41 units on a scale — p=0.26

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Role modeling in Shared medical appointments to Promote Establishing Collaborative Teams (ReSPECT) (Behavioral)
Age
Adult, Older Adult · 25+ yrs
Sex
All
Sponsor
US Department of Veterans Affairs
Primary completion
May 2013

Outcome Measures

OutcomeResultp-value
PRIMARY
Provider Abilities Scale - Subscale From the Midwest (MW) Clinicians' Network
7.09; 6.88 0.74
PRIMARY
Provider Abilities Scale - Subscale From the Midwest (MW) Clinicians' Network
7.09; 6.88 0.74
SECONDARY
Attitudes Toward Healthcare Teams Scale and Subscales
4.44; 4.24
SECONDARY
Attitudes Toward Healthcare Teams Scale and Subscales
4.44; 4.24

Summary

The investigators' study focuses on improving the care of diabetes, a complex chronic illness, by providing important insights into interprofessional training and its potential role in fostering the necessary interdisciplinary management needed for chronic conditions and in addressing the gap between best practice and actual care provided.

Eligibility Criteria

Inclusion Criteria

CLINICIANS

  • All clinicians in all of Ohio's CBOCs (except for the Georgetown CBOC) will be eligible for the study (all PCPs have patients with DM in their panel of patients).

PATIENTS

  • All diabetic patients who are seen in Ohio's CBOCs (except for the Georgetown CBOC) will be eligible for the study.

Exclusion Criteria

CLINICIANS

  • Any clinician who does not have diabetic patients on their panel, who aren't apart of Ohio's CBOC's, or see patients at the Georgetown CBOC will not be eligible to participate.

PATIENTS

  • Patients who don't have a diagnosis of diabetes, who aren't seen at one of Ohio's CBOC's, or is seen for their medical care at the Georgetown CBOC will not be eligible to participate.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00854594). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search