Self-Management and Resourceful Transition of Type 2 Diabetes With Stage 3 Kidney Disease

NCT ID: NCT01067963

Last Updated: 2015-06-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-12-31

Study Completion Date

2012-10-31

Brief Summary

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The purpose of this study is to establish the usefulness and the impact of a tailored behavioral-education and counseling intervention titled Self-Management and Resourceful Transition (S.M.a.R.T) among patients with type 2 diabetes mellitus and stage 3 chronic kidney disease, in order to help them to manage their behaviors related to their condition and health.

Detailed Description

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The SMaRT intervention is a 3-week intervention that uses a combined behavioral-education and counseling methodology. The combined intervention involves computer-aided education alongside telephone counseling via motivational interviewing. The computer-aided education is tailored to the diagnoses of type 2 diabetes and chronic kidney disease and designed in a learning module approach to facilitate goal-setting and discussion of health concerns with greater efficacy and in a more informed way during the brief office visit. Such Computer-aided education has been used to improve diabetes self-management and glycemic control in middle-aged to older adults with moderate success. The inclusion of CKD information will augment current diabetes self-management intervention. The telephone counseling using the evidence-based behavioral change approach of motivational interviewing is a patient-centered approach of partnering with patients by eliciting their health-related concerns. This approach tailors the SMaRT intervention to include collaborative goal-setting with guidance based upon the patient's readiness for change.

Conditions

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Diabetes Mellitus, Type 2 Renal Insufficiency, Chronic

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Behavioral-education/counseling

Computer assisted education and telephone counseling using motivational interviewing.

Computer assisted education and motivational interviewing

Group Type EXPERIMENTAL

Computer assisted education and motivational interviewing.

Intervention Type BEHAVIORAL

9 study contact points. 3-week intervention using computer-assisted learning modules and telephone counseling using motivational interviewing.

Group talks/social chat

Group session talks on general topics about healthy lifestyle, printed power point handouts, telephone calls comprised of social conversation to discuss the handout content.

Group Type PLACEBO_COMPARATOR

Group talks/social chat

Intervention Type BEHAVIORAL

9 study contact points. 3 group talk session on general topics about healthy lifestyle, printed power point handouts, telephone calls comprised of social conversation to discuss the handout content.

Interventions

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Computer assisted education and motivational interviewing.

9 study contact points. 3-week intervention using computer-assisted learning modules and telephone counseling using motivational interviewing.

Intervention Type BEHAVIORAL

Group talks/social chat

9 study contact points. 3 group talk session on general topics about healthy lifestyle, printed power point handouts, telephone calls comprised of social conversation to discuss the handout content.

Intervention Type BEHAVIORAL

Other Intervention Names

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Experimental Group Attention Control Group

Eligibility Criteria

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Inclusion Criteria

* Diagnosed Type 2 Diabetes
* 18-85 years old
* Stage 3 Chronic Kidney Disease
* Speaks and reads English

Exclusion Criteria

* Hypoglycemia with 3rd party treatment in past 3 months
* Type 1 Diabetes
* On Dialysis
* Does not speak English
* Factors likely to preclude protocol adherence
Minimum Eligible Age

18 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Robert Wood Johnson Foundation

OTHER

Sponsor Role collaborator

National Center for Research Resources (NCRR)

NIH

Sponsor Role collaborator

University of Colorado, Denver

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Teresa J. Sakraida, PhD, RN

Role: PRINCIPAL_INVESTIGATOR

University of Colorado Denver College of Nursing

Alkesh Jani, MD

Role: PRINCIPAL_INVESTIGATOR

University of Colorado Denver, School of Medicine and VA Eastern Colorado Hospital

Locations

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University of Colorado Hospital

Aurora, Colorado, United States

Site Status

VA Eastern Colorado Hospital

Denver, Colorado, United States

Site Status

Countries

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United States

References

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Other Identifiers

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1UL1RR025780

Identifier Type: NIH

Identifier Source: secondary_id

View Link

RWJ64198

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

08-0939

Identifier Type: -

Identifier Source: org_study_id

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