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N/A Completed N=70 Randomized Treatment

Multicomponent Telecare Model for Supporting Prediabetes Patients

Prediabetic State · Glucose Intolerance
Source: ClinicalTrials.gov NCT01671293 ↗
Enrolled (actual)
70
Serious AEs
0.0%
Results posted
Jun 2015
Primary outcomePrimary: Change From Baseline in Weight Parameter — -.58; -.18 kilograms

Summary

The purpose of this study is to determine whether a multi-component remote care model (telephone-based) is effective to achieve the modification of unhealthy eating practices and increase physical activity in adults who have prediabetes and over-weight/obesity. The effectiveness of the remote care model will be determined with respect to the mentioned practices as well as anthropometric parameters (Waist circumference and Weight) and clinical parameters (Fasting Glucose, Triglycerides, Total Cholesterol) which are sensitive to changes in these habits. The counseling intervention is the core of the multi-component tele-care model, which also includes counseling-through text messages, supply of Educational material and self-monitoring equipment (pedometers and measuring tape for patients to check their waist circumference).

Outcome Measures

OutcomeResultp-value
PRIMARY
Change From Baseline in Weight Parameter
-.58; -.18
SECONDARY
Change From Baseline in Self Report of Physical Activity
SECONDARY
Change From Baseline in Fasting Glucose
SECONDARY
Change From Baseline in Triglycerides
SECONDARY
Change From Baseline in Total Cholesterol
SECONDARY
Change From Baseline in Self Report of Dietary Practices
SECONDARY
Change of Baseline in Knowledge About Prediabetes
SECONDARY
Change of Baseline in Waist Circumference

Eligibility Criteria

Inclusion Criteria

  • Prediabetes diagnosis
  • 25- 34 Body Mass Index
  • cellphone

Exclusion Criteria

  • Fasting blood glucose ≥ 126 (at the beginning of the intervention).
  • Terminal chronic diseases
  • Major cardiovascular problems (ie: angina pectoris, myocardial infarction, cerebrovascular accident)
  • Severe psychiatric pathology
  • Presence of another pathology which, for the doctor assessing the patient (at the beginning of the intervention), can be a contraindications to participate in the program.
  • be pregnant
  • To belong to private health system (called ISAPRE).
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01671293). 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. Informational only — not medical advice.

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