lifestyle modification program in pre-diabetic individuals

Not Applicable

• Conditions: per-diabetic people.; Prediabetes; R73.03

• Registration Number: IRCT20171226038083N1
• Lead Sponsor: Ahvaz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 17 December 2019

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 242

Inclusion Criteria

Pre-diabetic people
Age of 30 to 75 years
Resident of Hovizeh

Exclusion Criteria

Acute or chronic comorbidities such as mental illness, mental retardation, chronic infectious disease (tb), or motor disability

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Hemoglobin A1c (HbA1c). Timepoint: Starting the study and 3 months later. Method of measurement: we use CERA-STAT 2000 Analyzer (CERAGEM MEDISYS inc).;Health-related quality of life (HR-Qol). Timepoint: At the base-line and the end of study (0 and 6-month). Method of measurement: Assessing the Quality of Life of the Diabetic patients by using the World Health Organization (WHO) Quality of Life Questionnaire:. Effect of Intervention.

Secondary Outcome Measures

Name	Time	Method
The patient's readiness to change in each of the three areas of the diet, physical activity and stress. Timepoint: Before intervention and after intervention. Method of measurement: A researcher-made questionnaire based on the PRECEDE PROCESS model that will be standardized in the study process.