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Comparison · NCT01977599-4e790adb

No Text Message Reminder (Control) Arm vs Text Message Reminder Arm: Mobile Prevalence

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. No Text Message Reminder (Control) Arm vs Text Message Reminder Arm: Mobile Prevalence. Trial comparisons, record NCT01977599-4e790adb. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01977599-4e790adb

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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 10.3890.3610.418wilson
Risk in group 20.4060.3780.435wilson
Risk difference, group 1 minus group 2-0.0173-0.05780.0232newcombe hybrid score
Risk ratio, group 1 over group 20.9570.8651.06log
Odds ratio, group 1 over group 20.930.7851.1log
Number needed to treat, for one fewer participant with the outcome on No Text Message Reminder (Control) Arm than on Text Message Reminder Arm57.7from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1No Text Message Reminder (Control) Arm
Control Arm, in which patients are invited to breast screening as per standard West of London Breast Screening Protocol (i.e. without a text message appointment reminder). Uptake of breast screening in this group will be compared with the text message reminder group to test for significant differences.
4351,118OG000
Group 2Text Message Reminder Arm
Patients randomly allocated to this arm of the study will be sent a text message reminding them of the time, date and venue of their breast screening appointment 48 hours in advance.~Text Message Reminder for Breast Screening Appointment: Non-clinical/administrative.
4561,122OG001

Outcome

Type
SECONDARY
Title
Mobile Prevalence
Description
Number of women with a valid mobile telephone number on the GP Clinical System
Time frame
The accuracy of patient mobile records was assessed for the intervention group at the time the text reminder was sent (i.e. 48 hours before the appointment). A check for the control group was performed at the same time.
Population

Source ClinicalTrials.gov

Trial

Title
Are Text Message Reminders an Effective Intervention for Improving the Uptake of Breast Screening?
NCT number
NCT01977599
Phases
NA
Conditions
Breast Screening
Interventions
Text Message Reminder for Breast Screening Appointment
Lead sponsor
Imperial College Healthcare NHS Trust
Results first posted
2021-04-06

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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