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Clinical Trials/NCT01510301
NCT01510301
Completed
Not Applicable

Mastery and Autonomy in Management of Hypertension With a Mobile Self-report System

Göteborg University1 site in 1 country51 target enrollmentMarch 2012
ConditionsHypertension

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hypertension
Sponsor
Göteborg University
Enrollment
51
Locations
1
Primary Endpoint
Adherence to antihypertensive medication
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
March 2012
End Date
June 2012
Last Updated
9 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Göteborg University
Responsible Party
Sponsor

Eligibility 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

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Adherence to antihypertensive medication

Time Frame: 8 weeks

Adherence to antihypertensive medication will be checked through a question in the cell phone and evaluation of patient´s use of antihypertensive medication will be checked from the National Prescribed Drug Register of drugs. Twenty patient-physician/nurse consultations will be audio/video-recorded at regularly scheduled appointments to obtain authentic evidence of the use of the self-reports in clinical practice. The outcomes will include blood pressure measurement, registration of self-reported symptoms and discourse analyses.

Secondary Outcomes

  • Systolic blood pressure(8 weeks)

Study Sites (1)

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