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Clinical Trials/NCT02682095
NCT02682095
Terminated
Not Applicable

Possibilities for Patients With Elevated Blood Pressure to Achieve Blood Pressure Control Without Affecting Quality of Life (the PEQ Study)

Eva Drevenhorn1 site in 1 country12 target enrollmentApril 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hypertension
Sponsor
Eva Drevenhorn
Enrollment
12
Locations
1
Primary Endpoint
Self-care agency
Status
Terminated
Last Updated
5 years ago

Overview

Brief Summary

The purpose of the study is to get an understanding about what problems patients with hypertension are facing, how they manage these challenges, how they feel and what requirements they believe are important to have in their treatment. These factors will later act as a foundation and incentive for designing an intervention that may result in more patients achieving blood pressure control with maintained quality of life.

Detailed Description

This is a Swedish observational mixed-methods study to get an understanding about what problems patients with hypertension are facing. The information will act as a foundation for designing an intervention/interventions that may result in more patients achieving blood pressure control with maintained quality of life. Patients, who have well/not well controlled blood pressure, are to fill in questionnaires about their view on ability to perform self-care and their perceived quality of life. Individual interviews will also be made about for what reasons they do or do not change lifestyle as well as take their drugs to treat their hypertension. In focus group interviews the patients are to be asked about what they want and expect in the encounter with health care personnel, what other things outside the health care area would be helpful for the patient and how age, gender, cultural and psychosocial aspects affect the ability to achieve blood pressure control. The developed future interventions will be evaluated in clinical practice.

Registry
clinicaltrials.gov
Start Date
April 2016
End Date
May 31, 2019
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Eva Drevenhorn
Responsible Party
Sponsor Investigator
Principal Investigator

Eva Drevenhorn

Senior Lecturer

Lund University

Eligibility Criteria

Inclusion Criteria

  • diagnosed with hypertension since 9 months
  • being able to read and speak Swedish

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Self-care agency

Time Frame: through study completion, an average of 6 months

Exercise of Self Care Agency (ESCA) instrument

Quality of life: SF-36

Time Frame: through study completion, an average of 6 months

Short Form Health Survey, 36 items

Focus-group interviews

Time Frame: through study completion, an average of 1 year

Discussions in focus-groups

Individual interviews

Time Frame: through study completion, an average of 3 months

Semistructured interviews

Study Sites (1)

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