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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04809519
Other study ID # 0030
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 6, 2021
Est. completion date January 21, 2022

Study information

Verified date February 2022
Source Akdeniz University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Purpose: The aim of this study is to evaluate the effect of multimodal interventions based on Integrative Nursing (IN) principles on blood pressure, stress, and hypertensive treatment compliance levels in individuals living in the community and with uncontrolled hypertension. Design: This is a single-center, 1:1 randomized, single-blind, parallel, active comparator trial. Method: Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT) Statement 2013 checklist is used in this study. In the study, the group in which Integrative Nursing Principles-Based Multimodal Interventions were applied (UHTINuM) was taken as the experimental (n: 24), the group in which health recommendations were given as the active comparator group (n: 24). The sample size calculated according to the reference study data is 62. However, this target number could not be reached due to the COVID-19 pandemic conditions. This study was carried out with adult individuals aged 50-65 in Hayat Park, which is located within the borders of Konyaaltı District of Antalya province. Multimodal interventions including 12-week meditation and breathing techniques, yoga, hypertension treatment compliance training, and home blood pressure measurement training were applied to the UHTINuM group. The control group was directed to a specialist doctor as an intervention, information notes for hypertensive individuals and standard brochures prepared by the Ministry of Health were given. The primary results of the study were measured using an aneroid and automatic blood pressure device (blood pressure measurement), Hill Bone Hypertension Treatment Adherence Scale, Perceived Stress Scale (PSS). This will be the first study to evaluate the effect of multimodal interventions based on integrative nursing principles in uncontrolled hypertensives. If the hypotheses of the study are reached, it is expected that the planned intervention protocol will be used by other researchers and thus become widespread in the literature. Also, the results will help contribute to the provision of care in terms of IN.


Recruitment information / eligibility

Status Completed
Enrollment 48
Est. completion date January 21, 2022
Est. primary completion date December 31, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 50 Years to 65 Years
Eligibility Inclusion Criteria: - Being diagnosed with hypertension and using regular medication for at least 1 year - Despite being diagnosed with hypertension, systolic blood pressure 140-159 diastolic blood pressure exceeding 90-99 mmHg - Being between the ages of 50-65 - Not being an obstacle to physical activity - Volunteering to participate in research Exclusion Criteria: - The individual is not at a cognitive level to answer the questions asked. - Having a mental illness that prevents the individual from participating in the initiative according to his / her own declaration. - Stage 2 hypertension (SBP> 160 mm Hg or diastolic blood pressure =100 mm Hg) - Having a renal problem and cardiovascular disease in which activity is prohibited by the specialist physician according to the statement of the individual. - BMI> 40 - Having practiced yoga once a month in the last 6 months Serious musculoskeletal problems such as spinal stenosis, which, according to the individual's statement, may limit participation in yoga. - The individual is using other mind-body therapies such as Qigong, tai chi or meditation.

Study Design


Intervention

Other:
Integrative Nursing based Multimodal Interventions for Uncontrolled Hypertensives
In this study, multimodal interventions including yoga, meditation, and breathing techniques, compliance training for hypertension treatment, and home blood pressure measurement training will be applied to the experimental group.
Ongoing treatment
The ongoing health service of the control group will continue. In addition, the control group will be directed to a specialist doctor and standard brochures prepared by the Ministry of Health for hypertensive individuals will be given.

Locations

Country Name City State
Turkey Community Social Area (Hayat Park) Antalya Konyaalti

Sponsors (1)

Lead Sponsor Collaborator
Akdeniz University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Blood Pressure Official and self-Blood Pressure Measurements For 12 weeks
Primary Perceived Stress Level Perceived Stress Scale: A minimum of 0 and a maximum of 32 points are obtained from the scale. Higher total score means higher perceived stress level. For 12 weeks
Primary Hypertensive Treatment Compliance Hill-Bone Compliance to High Blood Pressure Therapy Scale: The scale total score varies between 0 and 42 in relation to the number of items. The scores are evaluated for the interpretation of the total, medical, nutrition and interview sub-dimension compliance scores of the scale; If the person gets "0" points in total by giving the most positive answers to all questions, he / she is considered to be fully compatible. Change from Baseline Hypertensive Treatment Compliance at 12 months
Secondary Physical activity level International Physical Activity Questionnaire: The short form (seven questions) obtains information about walking, moderate and intense activities, and time spent sitting. The energy required for the activities is calculated by the MET minute score. The score obtained is classified as nonphysical (MET = 600 energy level), insufficient physical activity level (MET = 600-3000 energy level), and sufficient physical activity level (MET =3000 energy level). Change from Baseline Physical activity level at 12 months
Secondary BMI height and weight measurement Change from Baseline BMI at 12 months
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