- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06547879
Effect of a Daily Life Activity-Based Awareness Training Program on Hypertensive Individuals
Effect of an Education Program Based on the Roper, Logan, and Tierney Model of Daily Living Activities Supported With Mindfulness on Self Care, Treatment Adherence, and Healthy Lifestyle Behaviors in Hypertensive Individuals
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Considering that theory-based educational practices alone are not sufficient in the management of HT and that a multifaceted perspective must be developed, in addition to the education based on the ADL nursing model, the conscious awareness approach, which is effective in stress management with its easy integration into daily life, has also been included in this program. In this way, individuals can gain experience and reach self-awareness as a result of theory and skill-based training and feel more motivated to adopt healthy lifestyle behaviors. Multicomponent interventions offer a more comprehensive approach by combining a variety of methods, such as mindfulness, exercise, and dietary changes, as well as educational programs. Such integrated interventions can positively impact both individuals' knowledge and lifestyle habits, providing more effective results in the management of HT and contributing to long-term health improvements.
In this context, this study aimed to evaluate the effect of the training program, structured according to Roper, Logan and Tierney's ADL nursing model and supported by awareness, on self-care, treatment compliance and healthy lifestyle behaviors in individuals with HT. This research is the first randomized controlled study in which the effects of a training program that is suitable for our country's patient profile for HT self-management, shaped according to multidimensional and up-to-date guidelines, that can encourage participants to change behavior, are tested. It has the potential to provide unique contributions to the field with its potential to create infrastructure.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Ankara
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Altındağ, Ankara, Turkey, 06080
- Ornek Mahallesi, 2061. Caddesi 4/1 Blok No:37
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Aged between 18 and 65
- Literate (able to read and write)
- Followed up for at least 6 months with a diagnosis of stage 1 primary hypertension (HT)
- Taking at least one antihypertensive medication
- No changes in antihypertensive medication in the past month
- Able to use a smartphone and WhatsApp® application
- Having internet access and willing to participate in online sessions
Exclusion Criteria:
- Those with hearing and vision problems
- Those with cognitive impairment
- Having a psychiatric diagnosis such as major depression
- Having a history of major heart surgery in the last 6 months
- Those with severe symptom burden due to advanced COPD, heart failure, asthma, cancer
- Individuals who used another mind-body-based approach (yoga, meditation, relaxation exercise, etc.) during the research were not included in the sample.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control group
Usual care.
|
|
|
Experimental: Intervention group
One session per week; 20 minutes for the training module and 25 minutes for the awareness practice, a total of 45 minutes each week, for a total of 8 weeks.
|
The HT self-management training program was continued in the form of one session per week, a total of 8 modules, for 8 weeks, with different module content each week.
After these eight-week training and awareness sessions were completed, the implementation of the study was terminated (week 8), no additional intervention was given to the intervention group, and the evaluations at the 8th week (end of intervention-T1) and the 12th week (follow-up-T2) were carried out by the researcher during the routine checks of the participants at the outpatient clinic.
It was carried out face to face.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hypertension Self-Care Profile
Time Frame: At week 0, week 8 and week 12
|
The Hypertension Self-Care Profile Scale has three subscales: behavior, motivation and self-efficacy.
In this scale, each sub-dimension is evaluated separately and a total of minimum 20 and maximum 80 points can be obtained from the scale.
Higher scores indicate better self-care.
|
At week 0, week 8 and week 12
|
|
Hill-Bone Hypertension Treatment Compliance Scale
Time Frame: At week 0, week 8 and week 12
|
The scale consists of three sub-dimensions (interview, medical and nutrition) and a total of 14 questions.
The total score that can be obtained from the scale varies between 14 and 56; A score of 14 indicates full compliance, while higher scores indicate treatment non-compliance.
|
At week 0, week 8 and week 12
|
|
Healthy Lifestyle Behaviors Scale II
Time Frame: At week 0, week 8 and week 12
|
It aims to evaluate individuals' behaviors towards healthy lifestyles.
There are 52 items in total in the scale, and all of the items consist of positive expressions.
The minimum score that can be obtained from the scale is 52 and the maximum score is 208.
|
At week 0, week 8 and week 12
|
|
Conscious awareness
Time Frame: At week 0, week 8 and week 12
|
It evaluates individual differences in individuals' states of consciousness and measures their tendency to be aware of and pay attention to momentary experiences in daily life.
The total score that can be obtained varies between 15 and 90.
A high score indicates a high level of conscious awareness.
|
At week 0, week 8 and week 12
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Systolic and diastolic blood pressure
Time Frame: At week 0, week 8 and week 12
|
Blood pressure measurement by the researcher with a digital device.
|
At week 0, week 8 and week 12
|
|
Metabolic Control Variables
Time Frame: At week 0 and week 8
|
A total of 15 items regarding fasting blood sugar, HbA1c, urea, creatinine, uric acid, glomerular filtration rate, serum sodium and potassium values, lipid panel, hemogram, height, weight and BMI values.
|
At week 0 and week 8
|
|
Hypertension Information Assessment
Time Frame: At week 0 and week 8
|
Individuals' HT knowledge status before and after the intervention was evaluated and the data were classified as "correct" and "incorrect" and calculated as number-percentage.
|
At week 0 and week 8
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Hacer Eroğlu, haceroturmaz@hacettepe.edu.tr
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- record 4
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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