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The Effect of the Use of BATHE Interview Technique on Treatment Compliance in Hypertension Patients in Primary Care

Not Applicable
Completed
Conditions
Essential Hypertension
Interventions
Behavioral: BATHE
Registration Number
NCT05476120
Lead Sponsor
Dokuz Eylul University
Brief Summary

The research is planned to evaluate the treatment compliance after the BATHE interview technique in hypertension patients.

Detailed Description

In order to be evaluated for suitability for the study, patients aged 18-80 who have been diagnosed with hypertension for at least 6 months (n= 220) were interviewed and 86 hypertension patients who met the inclusion criteria and volunteered for the study were included in the study. Participants whose eligibility was determined as a result of the evaluation in terms of inclusion and exclusion criteria were asked about their volunteerism in the intervention study, their written consent was obtained from those who volunteered, and those who volunteered were randomized.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
2
Inclusion Criteria
  • Being a patient of hypertension
  • Be over 18 years old
  • Be less than 80 years old
  • To have been diagnosed for at least 6 months
  • Volunteering
  • To be able to use any of the online video calling channels
Exclusion Criteria
  • Communication problem
  • Presence of psychiatric illness and/or use of psychiatric medication
  • Pregnancy

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
BATHEBATHEIn each interview, the intervention group was intervened by the physician to increase compliance with the treatment using the BATHE technique, and brief information was given emphasizing the importance of drug compliance and lifestyle changes routinely applied by the Family Medicine Department in hypertension patients. The patients in the intervention group were interviewed face-to-face at the 0th and 6th months, and online at the 3rd month.
Primary Outcome Measures
NameTimeMethod
The Scale for Evaluating the Success of Treatment Adherence and Lifestyle Change in Hypertensive IndividualsBaseline and sixth month

The scale consists of 18 questions. The questions were structured in a positive and negative way and the answers were expressed as a five-point likert. The contents of the questions were prepared to enlighten the subjects of medical treatment and clinical controls, communication with the physician, active lifestyle and physical activity, weight control, healthy nutrition and salt consumption, and disease awareness. After reverse scoring, if all items are given 5 points, the highest total score that can be obtained from the scale is 90. When all items are given 1 point, the lowest score that can be obtained from the scale is 18. The scale cutoff point is 68. A score of less than 68 indicates low adherence to treatment, and a score of 68 and above indicates high adherence to treatment. An increase in the score on the scale indicates an increase in treatment compliance.

Turkish Modified Morisky ScaleBaseline and sixth month

The scale consists of 6 questions. The questions were answered as Yes/No and in the evaluation; in questions 2 and 5 yes 1 point, no 0 points; In other questions, yes is 0 points, no is 1 point. If the total score obtained by the patient in questions 1, 2 and 6 is 0 or 1, it indicates low motivation level, and \>1 indicates high motivation level. If the total score from questions 3, 4 and 5 is 0 or 1, it indicates low level of knowledge, and \>1 indicates high level of knowledge.

Secondary Outcome Measures
NameTimeMethod
BMIBaseline and sixth month

At the beginning and at the 6th month, BMI of the participants was measured by the researcher under appropriate conditions and in both interviews.

Waist circumferenceBaseline and sixth month

At the beginning and at the 6th month, the waist circumference of the participants was measured by the researcher under appropriate conditions and in both interviews.

Blood pressureBaseline and sixth month

In both interviews, both systolic and diastolic blood pressures of the participants were measured by the researcher under appropriate conditions and at 6 months.

Trial Locations

Locations (1)

Vildan MEVSİM

🇹🇷

İzmir, Balçova, Turkey

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