Actively Recruiting

Phase Not Applicable
Age: 65Years - 85Years
All Genders
Healthy Volunteers
ID07179887

Remote Ischaemic Conditioning in Older Adults and Its Effects on Dynamic Cerebral Autoregulation

Led by University of Nottingham · Updated on 2025-09-18

45

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

Sponsors

U

University of Nottingham

Lead Sponsor

U

University of Leicester

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are studying the effects of Remote Ischaemic Conditioning (RIC) on vascular health in older adults aged 65 to 85. RIC involves applying short periods of restricted blood flow to a limb to improve blood vessel function elsewhere in the body. This trial aims to determine whether increasing the intensity of RIC leads to greater improvements in biomarkers such as dynamic cerebral autoregulation (dCA), which helps regulate brain blood flow and has shown to improve with RIC in younger adults. Participants will be randomly assigned to receive one of three interventions for six weeks: daily RIC sessions, RIC sessions three times per week, or sham RIC sessions three times per week. Each session involves inflating a blood pressure cuff on a limb for four cycles of five minutes at 20 mmHg above systolic blood pressure, followed by five minutes of deflation. The sham group undergoes a similar procedure but with only 20 mmHg inflation. This design compares different RIC doses and a placebo to assess effects on vascular health. Participants will visit the research site at the beginning and end of the six weeks for evaluations including blood pressure measurements, assessments of cerebral autoregulation using ultrasound, and blood sample collection. Researchers will measure the autoregulatory index as the primary outcome and also assess blood pressure and blood plasma markers as secondary outcomes. The study includes monitoring adherence and safety throughout the trial period, with participation lasting about six weeks in total.

CONDITIONS

Brief Title

Remote Ischaemic Conditioning in the Older Person and Effects on Dynamic Cerebral Autoregulation

Who Can Participate

Age: 65Years - 85Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Participant is willing and able to give informed consent for participation in the study
  • Participant aged 65 to 85 years
  • Participant is able to perform Remote Ischaemic Conditioning independently at home
Not Eligible

You will not qualify if you...

  • Active cardiovascular or cerebrovascular disease with an acute event within the last 12 months
  • Atrial fibrillation or other significant arrhythmias
  • Peripheral vascular disease
  • Haemostatic disorders
  • Soft tissue injury or fracture to the upper limb
  • Pregnant or breastfeeding
  • History or current psychiatric illness
  • History or current neurological condition such as epilepsy
  • Inability to identify temporal window for transcranial doppler ultrasound at screening
  • Any condition or presentation deemed by the study clinician to exclude participation
  • Participation in a research study within the last 3 months involving invasive procedures or inconvenience allowance

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 6 weeks

Participants complete Remote Ischaemic Conditioning sessions at home using a blood pressure cuff. Sessions vary by group, with daily or three times weekly treatments over 6 weeks.

Daily or 3 times weekly sessions depending on group assignment

Follow-up

Duration - Short-term post-treatment

Participants have assessments to measure effects on cerebral autoregulation and vascular health after treatment completion.

2 visits (baseline and week 6 assessments)

Trial Site Locations

Total: 1 location

1

School of Medicine, University of Nottingham, Royal Derby Hospital Centre

Derby, Derbyshire, United Kingdom, DE22 3DT

Actively Recruiting

Loading map...

Research Team

H

Harry Keevil, MB BChir

T

Tim England, MBChB PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

3

Similar Trials

PhytoRx Families: A Pilot Test Study to Address Food Securit...

Diet, Healthy

Actively Recruiting

1 location

Effects of Progressive Barbell Strength Training on Cardiova...

Blood Pressure

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here

Published Research Related To This Trial

Effect of Remote Ischemic Conditioning vs Usual Care on Neurologic Function in Patients With Acute Moderate Ischemic Stroke: The RICAMIS Randomized Clinical Trial.

Hui-Sheng Chen, Yu Cui, Xiao-Qiu Li...

https://pubmed.ncbi.nlm.nih.gov/35972485

Chronic remote ischaemic conditioning in patients with symptomatic intracranial atherosclerotic stenosis (the RICA trial): a multicentre, randomised, double-blind sham-controlled trial in China.

Chengbei Hou, Jing Lan, Yinan Lin...

https://pubmed.ncbi.nlm.nih.gov/36354026

Remote ischemic perconditioning as an adjunct therapy to thrombolysis in patients with acute ischemic stroke: a randomized trial.

Kristina Dupont Hougaard, Niels Hjort, Dora Zeidler...

https://pubmed.ncbi.nlm.nih.gov/24203849

Regulation of cerebral blood flow in humans: physiology and clinical implications of autoregulation.

Jurgen A H R Claassen, Dick H J Thijssen, Ronney B Panerai...

https://pubmed.ncbi.nlm.nih.gov/33769101