EUCTR2016-003986-25-ES
Active, not recruiting
Phase 1
Impact of self-measurement of blood pressure and self-adjustment of antihypertensive medication in the control of hypertension and adherence to treatment. A pragmatic, randomized, controlled clinical trial (ADAMPA Study)
Instituto de Investigación Sanitaria INCLIVA0 sites458 target enrollmentMarch 17, 2017
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Arterial hypertension
- Sponsor
- Instituto de Investigación Sanitaria INCLIVA
- Enrollment
- 458
- Status
- Active, not recruiting
- Last Updated
- 5 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •\- 40 years or older
- •\- have a diagnosis of hypertension of any origin
- •\- have a TAS\> 145 or TAD\> 90 mm Hg on the baseline examination
- •\- voluntarily agree to participate in the study and sign the corresponding informed consent
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1\.2 Adults (18\-64 years) yes
- •F.1\.2\.1 Number of subjects for this age range 158
- •F.1\.3 Elderly (\>\=65 years) yes
- •F.1\.3\.1 Number of subjects for this age range 300
Exclusion Criteria
- •\- inability to self\-care of their blood pressure, understanding, performing and / or self\-adjusting of medication by the patient, including dementia or significant cognitive impairment at the discretion of the investigator performing the recruitment
- •\- history of orthostatic hypotension (fall\> 20 mm Hg in systolic arterial tension after the orthostatic position)
- •\- have a blood pressure\> 200 or diastolic blood pressure\> 100 mm Hg at baseline
- •\- being on treatment with more than 4 antihypertensive drugs
- •\- be included in another high blood pressure study or in a clinical trial
- •\- presence of tremor or neurological disease that makes it difficult to perform AMPA
- •\- presence of arrhythmia
- •\- presence of terminal illness
- •\- chronic incapacitation to leave your home
- •\- have had an acute cardiovascular event in the last 3 months
Outcomes
Primary Outcomes
Not specified
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