Actively Recruiting
The Effect of MediYoga on Sleep Quality, Blood Pressure, and Quality of Life in Older Adults with Hypertension:
Led by Herlev and Gentofte Hospital · Updated on 2024-11-13
180
Participants Needed
1
Research Sites
86 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this Randomized Controlled Trial is to test if an intervention consisting of Yoga can increase quality of sleep and health related quality of life and decrease BP. Secondary to explore and describe the implementation of a yoga intervention and the participants' experiences and perspectives on the intervention in a process evaluation. The main question it aims to contribute knowledge about intervention of Yoga in a home environment for individuals with hypertension aged 65 years or older. Participants will (if they got selected into one of the two interventions groups), participate in Yoga exercises delivered by an app for 2 times a week for 10 weeks. Researchers will compare the intervention groups with the control group to see if Medi yoga has an effect in older people with hypertension.
CONDITIONS
Official Title
The Effect of MediYoga on Sleep Quality, Blood Pressure, and Quality of Life in Older Adults with Hypertension:
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 65 years or older
- Diagnosed with hypertension
- Able to read and speak Danish
- Able to give informed consent
- No other health conditions preventing participation
- Owns or uses a smartphone or tablet
You will not qualify if you...
- Starting new antihypertension medication during the study
- Changes in antihypertension medication over 10% or switching drugs during the study
- Regular mindfulness or yoga practice within the last two years
- Diagnosed sleep disorders such as sleep apnea or narcolepsy
- Regular use of sleep medication
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Herlev and Gentofte Hospital
Herlev, Copenhagen, Denmark, 2730
Actively Recruiting
Research Team
K
Katrine Amdi, MSc
CONTACT
S
Signe Risom, associated Prof.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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