- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01849731
Effectiveness of Two Interventions in Patients With Low Educational Level With Diabetes to Reduce Inequalities in Self-care Behavior
May 6, 2013 updated by: Clara Bermúdez-Tamayo, Andalusian School of Public Health
The purpose of this cluster randomized trial is to determine whether an intervention implemented in a General Surgery, based in improving patient-provider communication, results in a better diabetes self-management in patients with lower educational level.
A secondary objective is to assess whether telephone reinforcement enhances the effect of such intervention.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
184
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
-
-
-
Granada, Spain, 18011
- Andalussian School of Public Health
-
-
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
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Diagnosis of DM2,
- Over 18 years,
- Low educational level (no college to GBS or ESO),
- Inadequate glycemic control (glycosylated hemoglobin levels above 7%)
Exclusion Criteria:
- Physical or mental condition that prevents the completion of the intervention - complications arising from severe DM2 altering routine medical monitoring.
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: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: Control Group
|
|
Experimental: Intervention A
Face-to face intervention
|
is carried out by the GPs during the clinic visit and consists of seven visits, one every three months.
Each session consists of completing a diabetes care record sheet (DCRS) together with the patient.
The DCRS consists of two parts: Five questions on self-care activities in the last three months and a graph with previously measured HbA1c levels.
This information is completed at each session, resulting in a graph showing the evolution of glycaemic control related to self-care activities.
The DCRS is explained patients, emphasising the relationship between self-care and glycemic control.
At the end of the session, patients are given a copy of the DCRS and suggested to show it and discuss it with their relatives.
|
Experimental: Intervention B
Face-to-face intervention plus telephone reinforcement
|
In this group patients receive the above described intervention A plus a telephone reinforcement It consists on five telephone calls lasting about 10 minutes each, to provide advice on carrying out physical exercise and eating a balanced diet and to encourage the use of health services related to diabetes control.
Any problems or doubts that patients have stemming from any aspect of diabetes care are also discussed.
Telephone reinforcement is carried out by a professional who has previously been trained in promoting T2DM self-management and in motivational interviewing techniques.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Glycosylated Haemoglobin levels
Time Frame: one year
|
one year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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.
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
February 1, 2011
Primary Completion (Actual)
December 1, 2012
Study Registration Dates
First Submitted
May 6, 2013
First Submitted That Met QC Criteria
May 6, 2013
First Posted (Estimate)
May 8, 2013
Study Record Updates
Last Update Posted (Estimate)
May 8, 2013
Last Update Submitted That Met QC Criteria
May 6, 2013
Last Verified
May 1, 2013
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- PI-0096-2010
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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