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Effects of Intense Aerobic Exercise on the Cerebrovascular Reserve Capacity in Patients With Hemodynamically Relevant Intra- and Extracranial Stenoses

Effects of Intense Aerobic Exercise on the Cerebrovascular Reserve Capacity in Patients With Hemodynamically Relevant Intra- and Extracranial Stenoses

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00912561
Acronym
Exercise
Enrollment
50
Registered
2009-06-03
Start date
2009-06-30
Completion date
2012-12-31
Last updated
2012-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stenosis

Keywords

chronic brain ischaemia, stroke prevention, exercise, physical training, Chronic, extra- or intracranial stenoses of brain supplying arteries

Brief summary

The purpose of this trial is to study the improvement of cerebral hemodynamics in high risk stroke patients with impaired Cerebrovascular Reserve (CVR) due to high grade stenosis of the internal carotid (ICA) or middle cerebral artery (MCA) by Intense Aerobic Exercise (IAEx).

Detailed description

The primary objective: Intense aerobic exercise (24/8 weeks) improves CVR \> 20% measured by Transcranial Doppler (TCD) in patients with hemodynamic relevant intra- or extracranial stenoses by enhanced cerebral arterio- and angiogenesis. Secondary objectives: Intense aerobic exercise (24/8 weeks) leads to: * an increase of Endothelial progenitor cell counts (EPCs) * qualitative and quantitative changes of endothelial markers and cytokines representing the inflammatory activity of atherosclerosis and neovascularisation * an improvement in cognitive performance and quality of life (QoL) * changes of the mean vessel size and of cerebral perfusion

Interventions

BEHAVIORALIntense aerobic exercise

3 Units (of at least 30 minutes) of intense aerobic exercise per week for 8 weeks

Sponsors

German Federal Ministry of Education and Research
CollaboratorOTHER_GOV
Gerhard Jan Jungehuelsing
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* high-grade stenosis of the intra- or extracranial ICA or the MCA with ipsilateral impairment of the CVR capacity measured by TCD

Exclusion criteria

* continuous physical activity ≥ 60 min/week within the last 3 months * cerebral bleeding or ischaemic stroke \< 3 months * contraindications for spiro-ergometry, IAEx, or MRI

Design outcomes

Primary

MeasureTime frame
change of cerebrovascular reserve capacityimmediately after intervention of 8 weeks, 3 months, 6 months, 12 months Follow up

Secondary

MeasureTime frame
Endothelial Progenitor Cells, cyto- and chemokinesafter intervention of 8 weeks, 3 months, 6 months, 12 months Follow up
Neuropsychological Testing/ Quality of lifeimmediately after intervention of 8 weeks, 3 months, 6 months, 12 months Follow up

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026