- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01972412
Telephone Use for Care of Persons With Diabetes Mellitus. (TCDM)
October 31, 2013 updated by: Tânia Alves Canata Becker, University of Sao Paulo
Telephone Support for Self-monitoring of Persons With Diabetes Mellitus Using the Chronic Care Model
The purpose of this study is to determine whether phone use contributes to diabetes control.
Study Overview
Detailed Description
Studies reinforce the need to test innovative care that can serve more patients, since education is a key element for the accession to the treatment of diabetes.
Recently, an innovative, feasible and low cost presented in the literature is the use of telephone support as an intervention strategy This study aims to evaluate the implementation of a telephone support for self-monitoring of people with diabetes mellitus treated in ribeirão Preto.
Study Type
Interventional
Enrollment (Anticipated)
296
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
São Paulo
-
Ribeirão Preto, São Paulo, Brazil, 14040-902
- Recruiting
- University of São Paulo at Ribeirão Preto College of Nursing
-
Contact:
- Carla Regina S Teixeira, Doctor
- Phone Number: 551636023434
- Email: carlarst@eerp.usp.br
-
Principal Investigator:
- Tânia A Canata Becker, Master
-
Ribeirão Preto, São Paulo, Brazil
- Recruiting
- Universidade de São Paulo
-
Contact:
- Carla Regina S Teixeira, Doctor
- Phone Number: 551636023434
- Email: carlarst@eerp.usp.br
-
Principal Investigator:
- Tânia A Canata Becker, Master
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- diabetes mellitus type 2
- age
- ability to listen and answer questions
Exclusion Criteria:
- often present less than 75% participation in the proposed activities
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Telephone support
Intervention type: Telephone support for four months.
|
Telephone support for four months about healthy diet, physical activity and medication use.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Telephone Support for self-monitoring of persons with diabetes mellitus using the Chronic Care Model
Time Frame: Four months
|
Four months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Tânia A Canata Becker, Master, University of São Paulo at Ribeirão Preto College of Nursing
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
April 1, 2013
Primary Completion (Anticipated)
January 1, 2014
Study Completion (Anticipated)
March 1, 2014
Study Registration Dates
First Submitted
March 26, 2013
First Submitted That Met QC Criteria
October 24, 2013
First Posted (Estimate)
October 30, 2013
Study Record Updates
Last Update Posted (Estimate)
November 3, 2013
Last Update Submitted That Met QC Criteria
October 31, 2013
Last Verified
October 1, 2013
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- EERP - 146.171
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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