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Comparison · NCT01907269-0f793264

Video-based Intervention vs Usual Care: Number of Participants That Initiate an Osteoporosis Prescription Medication

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. Video-based Intervention vs Usual Care: Number of Participants That Initiate an Osteoporosis Prescription Medication. Trial comparisons, record NCT01907269-0f793264. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01907269-0f793264

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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 10.1150.09840.135wilson
Risk in group 20.1050.0890.123wilson
Risk difference, group 1 minus group 20.0106-0.01430.0357newcombe hybrid score
Risk ratio, group 1 over group 21.10.8781.38log
Odds ratio, group 1 over group 21.110.8651.44log
Number needed to treat, for one more participant with the outcome on Video-based Intervention than on Usual Care93.9from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: usual care.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Video-based Intervention
Video-based intervention providing personalized feedback regarding patients' risk of subsequent fractures, customized information regarding osteoporosis care, and messaging to activate patients to become more engaged in improving osteoporosis treatment and doctor-patient communication. This novel content will use story-telling delivered via the Internet and DVDs. The content will be uniquely tailored to each person based on their reported barriers to care, age and race/ethnicity. The video-based intervention materials will be augmented by a personal phone call and interactive voice response messaging.~Video-based Intervention: Video clips delivered by DVD and Internet
1361,178OG000
Group 2Usual Care1311,250OG001

Outcome

Type
SECONDARY
Title
Number of Participants That Initiate an Osteoporosis Prescription Medication
Description
We will assess the number of participants that self-report the initiation of an osteoporosis prescription medication. It will be assessed using a self-completed survey. Osteoporosis prescription medications that will be assessed include: alendronate, calcitonin, denosumab ibandronate, raloxifene, risedronate, teriparatide, and zoledronic acid. We will not include initiation of estrogen hormone therapies as part of the outcome.
Time frame
18 months
Population

Source ClinicalTrials.gov

Trial

Title
A Direct-to-patient Intervention to Increase Rates of Osteoporosis Care
NCT number
NCT01907269
Phases
NA
Conditions
Osteoporosis
Interventions
Video-based Intervention
Lead sponsor
University of Alabama at Birmingham
Results first posted
2018-06-26

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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