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NCT06303206Not yet recruiting

TEC4Home Blood Pressure Randomized Controlled Trial

Telehealth for Emergency-Community Continuity of Care Connectivity Via Home Telemonitoring for Blood Pressure Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 12 Mar 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The goal of this clinical trial is to evaluate the effect of home blood pressure telemonitoring (HBPT) and case management (CM), relative to usual care, for improving blood pressure (BP) control among patients with high blood pressure discharged from the emergency department (ED). The main question it aims to answer is: Does telemonitoring with case management improve BP control, relative to usual care, for people with high blood pressure discharged from the ED? Secondary research questions will address: 1. How do these interventions (telemonitoring and case management) improve medication adherence? 2. Do these interventions reduce physician and ED visits? 3. Are these interventions safe? 4. How do these interventions influence patient experience? Participants in the intervention group will receive training and use of a home BP telemonitor with tele-transmission function for 12-months plus pharmacist case management to provide behavioral counseling, facilitate medication adherence, review telemonitored BP data, and adjust medications. The control group will receive usual care from their primary care physician and will receive the same home BP monitor and hypertension education.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
408 (estimated)
First submitted
4 Mar 2024
Start date
1 Jun 2024
Primary completion date
1 Jan 2027
Lead sponsor
University of British Columbia
NCT number
NCT06303206

What you commit to

  • Study type: Interventional
  • Planned participants: 408
  • From 1 Jun 2024 to the primary completion date, 1 Jan 2027
  • No sites listed in no 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.

Prior treatment

  • Acute surgical or trauma patients

Other illness

  • Hypertensive emergencies with evidence of end-organ damage, stroke, or acute coronary syndrome
  • Advanced cognitive impairment

Other

  • Pregnant women
  • Acute intoxication
  • Psychiatrically unstable patients
  • Patient requiring admission to hospital
  • Inability to use or care for home BP monitor correctly
  • From nursing home
  • Unstable housing
  • Non-English speaking or no family members who can help translate

Who the study is looking for

  • Adult patients aged ≥ 18 years of age
  • Elevated triage BP AND increased average BP in three subsequent repeated measurements that are spaced at least 30 minutes after triage (systolic BP ≥ 160 mm Hg or diastolic BP ≥ 100 mm Hg)
  • Own a smart phone
  • Willing to measure and tele-transmit home BP readings

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

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