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Motivational Interviewing Effects on Hypertensive Patients

Motivational Interviewing Effects on Hypertensive Patients attended to health centers of Gorgan city in 2014

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014113017736N3
Enrollment
140
Registered
2014-12-15
Start date
2014-02-05
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy lifestyle. Maltreatment NOS

Interventions

Intervention 1: Control group: the content of this group included the recommendations and information in terms of change healthy lifestyle and adherence to treatment that conducted by a health center
Lifestyle
Control group: the content of this group included the recommendations and information in terms of change healthy lifestyle and adherence to treatment that conducted by a health center staff using a le
Motivational interviewing group: the intervention was done through a psychologist who was authorized, each group ranged from 7 to 10 subjects that trained for 6 sessions over six months (45 to 60 minu

Sponsors

Golestan University of Medical Science (Technology and Information Department)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 139 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria were as follows: 1) patients diagnosed with hypertension by a physician; 2) patients who received one antihypertensive medication at least; 3) patients who agreed to participate in the survey and more than 18 years old. Excluded criteria were as: 1) pregnant women and being pregnant during the study and 2) secondary hypertensive patients.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The laboratory and clinical indices (systolic blood pressure, the diastolic blood pressure, triglyceride level and total cholesterol, the symptoms of hypertension, and the complications of hypertension). Timepoint: Baseline (pre-test). Method of measurement: Laboratory and clinical sheet.;Blood pressure. Timepoint: Baseline (pre-test). Method of measurement: Blood test, when patient in sitting position, 5 minutes after sitting from the left arm.;Treatment Adherence. Timepoint: Baseline (pre-test). Method of measurement: Treatment Adherence Questionnaire of Patients with Hypertension (TAQPH).;Demographic status (included age, gender, marital status, educational level and diagnosis duration). Timepoint: Baseline (pre-test). Method of measurement: Demographic questionnaire.;Self-efficacy. Timepoint: Baseline (pre-test). Method of measurement: General Self-Efficacy Scale (GSES).;Quality of life. Timepoint: Baseline (pre-test). Method of measurement: Medical outcomes study 36- item short form (SF-36).

Secondary

MeasureTime frame
Quality of life. Timepoint: Follow-up after 6 month. Method of measurement: Medical outcomes study 36- item short form (SF-36).;Self-efficacy. Timepoint: Follow-up after 6 month. Method of measurement: General Self-Efficacy Scale (GSES).;Treatment Adherence. Timepoint: Follow-up after 6 month. Method of measurement: Treatment Adherence Questionnaire of Patients with Hypertension (TAQPH).;The laboratory and clinical indices (systolic blood pressure, the diastolic blood pressure, triglyceride level and total cholesterol, the symptoms of hypertension, and the complications of hypertension(. Timepoint: Follow-up after 6 month. Method of measurement: Laboratory and clinical sheet.;Blood pressure. Timepoint: Follow-up after 6 month. Method of measurement: Blood test, when patient in sitting position, 5 minutes after sitting from the left arm.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyyed Kamal Mirkarimi

Golestan University of Medical Science

k.mirkarimi@goums.ac.ir+98 17 3253 2872

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026