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Comparison · NCT01795833-bf94b72f

Text Messages vs Control: Number of Participants With Progression to Type 2 Diabetes

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Text Messages vs Control: Number of Participants With Progression to Type 2 Diabetes. Trial comparisons, record NCT01795833-bf94b72f. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01795833-bf94b72f

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.210.1860.235wilson
Risk in group 20.2270.2020.254wilson
Risk difference, group 1 minus group 2-0.0175-0.05310.0182newcombe hybrid score
Risk ratio, group 1 over group 20.9230.7841.09log
Odds ratio, group 1 over group 20.9030.7321.11log
Number needed to treat, for one fewer participant with the outcome on Text Messages than on Control57.3from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: control.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Text Messages
Short text messages related to healthy lifestyle will be sent to half the subjects three times per week, in addition to one off 'one-to-one structured education' during the study period.~Short text messages: In addition to structured education on healthy lifestyle provided at baseline, subjects in the arm will receive short text messages containing educational, motivational and supportive content on diet, physical activity, and smoking (if appropriate) during the study period. The content will be appropriate to the stage of the transtheoretical model of behavioural change that the subject is in. This will be assessed by questionnaire at each visit to clinic.
2161,031OG000
Group 2ControlHalf of the subjects who has received only one off 'one-to-one structured education about healthy lifestyle during the study period2341,031OG001

Outcome

Type
PRIMARY
Title
Number of Participants With Progression to Type 2 Diabetes
Description
The primary outcome will be progression to type 2 diabetes as measured by HbA1c at baseline, 6 months, 12 months and 24 months or by any validated criteria in any other care setting. the World health Organization (WHO) / International Diabetes Federation (IDF) criteria for diagnosis of diabetes will be used throughout.
Time frame
24 months
Population

Source ClinicalTrials.gov

Trial

Title
Diabetes Prevention Using SMS Technology
NCT number
NCT01795833
Phases
NA
Conditions
Prediabetes
Interventions
Short text messages
Lead sponsor
Imperial College London
Results first posted
2019-11-12

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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