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NCT03973931Completed

Personalized Patient Data and Behavioral Nudges to Improve Adherence to Chronic Cardiovascular Medications

Personalized Patient Data and Behavioral Nudges to Improve Adherence to Chronic Cardiovascular Medications (The Nudge Study)

Source: ClinicalTrials.gov · Last updated 2 Apr 2025

Brief summary (registry, in English)

The study plans to learn if sending different text messages, serving as reminders or encouragement, may help patients take their medication more often if they have had trouble keeping up with their medicines.

Status (registry)
Completed
Study type
Interventional
Enrollment
9501 (actual)
First submitted
31 May 2019
Start date
1 Jul 2019
Primary completion date
25 May 2023
Lead sponsor
University of Colorado, Denver
NCT number
NCT03973931

What you commit to

  • Study type: Interventional
  • Participants enrolled: 9501
  • From 1 Jul 2019 to the primary completion date, 25 May 2023
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Patients who do not have a mailing address listed in EHR;
  • Patients who do not have a landline or cellphone listed in EHR;
  • Currently pregnant if denoted in the EHR at the time of the data pull;
  • Patients with a mailing address outside of the state of Colorado;
  • Patients that do not speak either English or Spanish.

Who the study is looking for

  • Patients with the following cardiovascular conditions and respective medication classes:
  • Hypertension (Beta-blockers \[B-blockers)\], Calcium Channel Blocker \[CCB\], Angiotensin converting enzyme inhibitors (ACEi), Angiotensin Receptor Blockers \[ARB\], or Thiazide diuretic)
  • Hyperlipidemia (HMG CoA reductase inhibitor \[Statins\])
  • Diabetes (Alpha-glucosidase inhibitors, Biguanides, DPP-4 inhibitors, Sodium glucose transport inhibitor, Meglitinides, Sulfonylureas, Thiazolidinediones, or statins Coronary artery disease P2Y12 inhibitor \[Clopidogrel, Ticagrelor, Prasugrel, Ticlopidine\], B-blockers, ACEi or ARB or statins)
  • Atrial fibrillation (Direct oral anticoagulants, B-blockers, CCB)

Age in the registry: 18 years to 89 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
UCHealth
Coordinator of this site? Confirm its status
AuroraUnited StatesUnknown status
University of Colorado Denver
Coordinator of this site? Confirm its status
AuroraUnited StatesUnknown status
VA Eastern Colorado Health Care System
Coordinator of this site? Confirm its status
AuroraUnited StatesUnknown status
Denver Health and Hospital Authority
Coordinator of this site? Confirm its status
DenverUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.