NCT Number: NCT02848547
Post Trial Analysis of a Primary Prevention Study in Asian Indians
An extended follow-up study of NCT00819455 conducted 5 years post randomization. In this study we estimate the incidence of type 2 diabetes among participants enrolled in the diabetes prevention programme. This will provide comparison of the progression to diabetes among group motivated through text messages and the group educated only during enrollment. A total of 537 participants were enrolled in the primary study and are invited to participate in a follow-up visit 3 years post active trial period.
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Notify MeKey information
Conditions
Age range
40 year–63 year
Sex eligibility
All sexes
Study type
Observational
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Participants of the primary prevention programme - NCT00819455.
Exclusion criteria
Unwilling for participation
Treatment and study plan
Primary outcomes
-
Incidence of type 2 diabetes among participants enrolled in the diabetes prevention programme.
Time frame: Two years
Secondary outcomes
-
Long-term impact of healthy lifestyle through mobile phone based text messaging
Time frame: Two years
Sponsors and collaborators
Lead sponsor
India Diabetes Research Foundation & Dr. A. Ramachandran's Diabetes Hospitals
Other
Registry information
Official study title
The Role of Information Technology in the Prevention of Type 2 Diabetes - An Extended Follow-up Study
Important dates
- Study start
- 2016
- Primary completion
- 2016
- Study completion
- 2016
- First posted
- Jul 28, 2016
- Registry last updated
- Aug 2, 2016
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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