Mobile Phone in Hypertension Management

Göteborg University

Status: Completed

Conditions: Hypertension

Treatments: Device: Mobile phone-based self-report system, electronic Patient-Reported Outcomes Measure (e-PROM)

Study type: Interventional

Funder types: Other

Identifiers

NCT01510301

MIHM

Details and patient eligibility

About

The purpose of this study is to examine if a mobile phone-based self-report system, using the patient's own mobile phone, will improve adherence to treatment of hypertension and lead to personal involvement of the patient in the treatment.

Enrollment: 51 patients

Sex: All

Ages: 30+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• Diagnosis of arterial hypertension
• Prescribed antihypertensive treatment
• Alert and oriented
• Swedish-speaking
• Access to a functioning cell phone
• Agreeing to regular controls at the National Prescribed Drug Register of drugs

Trial design

Primary purpose: Supportive Care

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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51 participants in 1 patient group

Self-report

Other group

Treatment:

Device: Mobile phone-based self-report system, electronic Patient-Reported Outcomes Measure (e-PROM)