Hypertension Clinical Trial
Official title:
Effect of Mat Pilates Training on Blood Pressure of Hypertensive Individuals
| Verified date | April 2014 |
| Source | Federal University of São Paulo |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | Brazil: Ethics Committee |
| Study type | Interventional |
The study aimed to evaluate the chronic effects of Mat Pilates Training on blood pressure, heart rate, double product and psychobiological factors in hypertensive medicated women and acute effects of Mat Pilates Exercise on blood pressure of such individuals.
| Status | Completed |
| Enrollment | 44 |
| Est. completion date | December 2013 |
| Est. primary completion date | December 2013 |
| Accepts healthy volunteers | No |
| Gender | Female |
| Age group | 30 Years to 59 Years |
| Eligibility |
Inclusion Criteria: - Hypertensives women - Age 30 to 59 years - Nonactive - Make use of antihypertensive medication Exclusion Criteria: - Orthopedic problems or other problem that prevented the exercises - Change in drug treatment during protocol - Absence in more than 25% of the exercise sessions |
Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| Brazil | Federal University of Sao Paulo | Santos | SP |
| Lead Sponsor | Collaborator |
|---|---|
| Federal University of São Paulo | Fundação de Amparo à Pesquisa do Estado de São Paulo |
Brazil,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Blood pressure | Blood pressure was measured by Ambulatorial Monitoring Blood Pressure before and after trial period and by semiautomatic monitoring before and after a single session of Mat Pilates exercise. | 16 weeks | Yes |
| Secondary | Heart Rate | Heart Rate was measured by Ambulatorial Monitoring Blood Pressure before and after trial period and by semiautomatic monitoring before and after a single session of Mat Pilates exercise. | 16 weeks | Yes |
| Secondary | Anxiety | Anxiety was analyzed by State-Trait Anxiety Inventory (STAI), before and after trial period. | 16 weeks. | Yes |
| Secondary | Stress | Stress was analysed by perceived stress questionnaire, before and after trial period. | 16 weeks | Yes |
| Secondary | Depression | Depression was analysed by Beck's Depression Inventory (BDI), before and after trial period. | 16 weeks | Yes |
| Secondary | Sleep quality | Sleep quality was analysed by The Pittsburgh Sleep Quality Index (PSQI), before and after trial period. | 16 weeks | Yes |
| Secondary | Perception of Sleep | Perception of Sleep was analysed by Mini Sleep Questionnaire, before and after trial period. | 16 weeks | Yes |
| Secondary | Sleepiness | Sleepiness was analysed by Epworth Sleepiness Scale, before and after trial period. | 16 weeks | Yes |
| Secondary | Quality of Life | Quality of Life was analysed by Questionnaire for Health-Related Quality of Life assessment of hypertensive patients, before and after trial period. | 16 weeks | Yes |
| Secondary | Flexibility | Flexibility was analysed by Bank of wells, before and after trial period. | 16 weeks | Yes |
| Secondary | Strength | Strength was analysed by hydraulic handgrip dynamometer, before and after trial period. | 16 weeks | Yes |
| Secondary | Body weight | 16 weeks | Yes | |
| Secondary | Height | 16 weeks | Yes | |
| Secondary | Waist circumference | 16 weeks | Yes | |
| Secondary | Hip circumference | 16 weeks | Yes |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Terminated |
NCT04591808 -
Efficacy and Safety of Atorvastatin + Perindopril Fixed-Dose Combination S05167 in Adult Patients With Arterial Hypertension and Dyslipidemia
|
Phase 3 | |
| Recruiting |
NCT04515303 -
Digital Intervention Participation in DASH
|
||
| Completed |
NCT05433233 -
Effects of Lifestyle Walking on Blood Pressure in Older Adults With Hypertension
|
N/A | |
| Completed |
NCT05491642 -
A Study in Male and Female Participants (After Menopause) With Mild to Moderate High Blood Pressure to Learn How Safe the Study Treatment BAY3283142 is, How it Affects the Body and How it Moves Into, Through and Out of the Body After Taking Single and Multiple Doses
|
Phase 1 | |
| Completed |
NCT03093532 -
A Hypertension Emergency Department Intervention Aimed at Decreasing Disparities
|
N/A | |
| Completed |
NCT04507867 -
Effect of a NSS to Reduce Complications in Patients With Covid-19 and Comorbidities in Stage III
|
N/A | |
| Completed |
NCT05529147 -
The Effects of Medication Induced Blood Pressure Reduction on Cerebral Hemodynamics in Hypertensive Frail Elderly
|
||
| Recruiting |
NCT06363097 -
Urinary Uromodulin, Dietary Sodium Intake and Ambulatory Blood Pressure in Patients With Chronic Kidney Disease
|
||
| Recruiting |
NCT05976230 -
Special Drug Use Surveillance of Entresto Tablets (Hypertension)
|
||
| Completed |
NCT06008015 -
A Study to Evaluate the Pharmacokinetics and the Safety After Administration of "BR1015" and Co-administration of "BR1015-1" and "BR1015-2" Under Fed Conditions in Healthy Volunteers
|
Phase 1 | |
| Completed |
NCT05387174 -
Nursing Intervention in Two Risk Factors of the Metabolic Syndrome and Quality of Life in the Climacteric Period
|
N/A | |
| Completed |
NCT04082585 -
Total Health Improvement Program Research Project
|
||
| Recruiting |
NCT05121337 -
Groceries for Black Residents of Boston to Stop Hypertension Among Adults Without Treated Hypertension
|
N/A | |
| Withdrawn |
NCT04922424 -
Mechanisms and Interventions to Address Cardiovascular Risk of Gender-affirming Hormone Therapy in Trans Men
|
Phase 1 | |
| Active, not recruiting |
NCT05062161 -
Sleep Duration and Blood Pressure During Sleep
|
N/A | |
| Not yet recruiting |
NCT05038774 -
Educational Intervention for Hypertension Management
|
N/A | |
| Completed |
NCT05087290 -
LOnger-term Effects of COVID-19 INfection on Blood Vessels And Blood pRessure (LOCHINVAR)
|
||
| Completed |
NCT05621694 -
Exploring Oxytocin Response to Meditative Movement
|
N/A | |
| Completed |
NCT05688917 -
Green Coffee Effect on Metabolic Syndrome
|
N/A | |
| Recruiting |
NCT05575453 -
OPTIMA-BP: Empowering PaTients in MAnaging Blood Pressure
|
N/A |