Recruiting
Phase 3

Health Coaching

Sponsor:

York University

Code:

NCT02036892

Conditions

Type 2 Diabetes

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Interventions

Lifestyle counseling with smartphone

Lifestyle counseling

Study Details

Brief summary:

Patients with Type 2 Diabetes randomly allocated to the intervention arm (health coaching + smartphone-based health promotion software) will have significantly better Hemoglobin A1c levels at 6 months post-intervention than patients with Type 2 Diabetes allocated to the control arm (health coaching alone).

Conditions

Type 2 Diabetes

Study ID

NCT02036892

Start date

Feb, 2012

Status verified date

Jan, 2014

Completion date

Jun, 2014

Anticipated

Primary completion date

May, 2014

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Clinical diagnosis of Type 2 Diabetes
  • Fluency in English and/or Spanish

Exclusion Criteria:

  • > 75 years of age

Study Design

Enrollment

115 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Lifestyle counseling with smartphones

Lifestyle counseling assisted by smartphones

active comparator: Lifestyle counseling

Lifestyle counseling

Interventions

Lifestyle counseling with smartphone

Lifestyle counseling with health promoting smartphone software

Lifestyle counseling

Lifestyle counseling

Primary outcome measure

  • Hemoglobin A1c [ Time Frame: 6 months follow up from baseline ]

Central Contacts and Locations

Central contacts

Locations

Black Creek Community Health Centre

Recruiting

Toronto, Ontario, Canada, M3M1A4

Contacts

More Information

Sponsor

York University

Last update posted

Jan 15, 2014

Last verified

Jan, 2014

Keywords

  • Diabetes

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by York University on 2014-01-15.