ClinicalTrials.Veeva

Menu

Understanding Cerebral Blood Flow Dynamics for Alzheimer's Disease Prevention Through Exercise (flADex)

U

University of Granada (UGR)

Status

Completed

Conditions

Blood Flow
Cerebrovascular Circulation
Cognitive Function 1, Social
Healthy Aging

Treatments

Behavioral: Resistance exercise condition
Behavioral: Aerobic exercise condition

Study type

Interventional

Funder types

Other

Identifiers

NCT06584656
PID2022-137399OB-I0

Details and patient eligibility

About

Dementia is one of the leading causes of disability worldwide. Underlying biological mechanisms are crucial in preclinical stages of Alzheimer's disease (AD). Alterations in cerebral blood flow (CBF) and their relationship with AD blood-based biomarkers may be fundamental at early stages of the pathology. Physical exercise is a trigger to modify these biological mechanisms. Therefore, flADex aims to examine the acute effects of different types of exercise (resistance vs. aerobic vs. control) on CBF, AD blood-based biomarkers, and its cognitive implications in older adults. The hypothesis is that acute resistance or aerobic exercise will fluctuate levels of blood-based biomarkers, and will exert acute CBF changes combined with cognitive implications.

Full description

The aging population is at an increasing risk of developing Alzheimer's Disease (AD), which is characterized by cognitive decline and memory loss. Current pharmacological treatments have targeted amyloid-beta (Aβ) and tau protein, and have largely failed to halt or reverse the progression of AD. This has led to a growing interest on examining additional underlying mechanisms responsible for the initiation of AD pathology in this preclinical stage, such as cerebral blood flow (CBF) alterations or peripheral levels of AD blood-based biomarkers. Parallelly, exercise might act as a trigger for these potential underlying mechanisms of AD in older adults. Thus, this study seeks to explore the acute effects of different type of exercise on CBF, blood-based biomarkers, and its cognitive implications in older adults.

FlADex is a counterbalanced crossover trial that will include 20 adults aged 68 to 83 with non-pathological brain amyloid status (<12 centiloid) and APOE e4 noncarriers. Each participant will be included in all study conditions in a randomized order: (i) moderate aerobic exercise (between 60-70 of the Maximal Heart Rate (HRmax); (ii); resistance exercise (4-6 Moderate intensity of Rate of Perceived Exertion) and (iii) control resting condition. Each condition, lasting 30 minutes, will be performed once. CBF will be assessed by magnetic resonance imaging using pseudo-continuous arterial spin labeling at pre-condition and at 3 consecutive times post-condition (at 20', 27' and 34' min). Blood-based biomarkers (Aβ42, Aβ40, p-tau217, p-tau181, GFAP, NfL, BDNF, IGF-1) will be measured pre-condition and post-condition (at 0', 50', 70' min). Cognitive outcomes (Flanker Test and Picture Sequence Memory Test) and mood status (feeling scale and POMS questionnaire) will be measured pre and post condition.

FlADex trial will shed light on the acute effects of different types of exercises on CBF and AD blood-based biomarkers before beta-amyloid accumulation. We expect that aerobic and resistance exercise will have different effects on CBF dynamics and AD blood biomarker levels over time in older adults

Enrollment

20 patients

Sex

All

Ages

68 to 83 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Older adults
  • Aged 68-83 years
  • Non-pathological cerebral beta-amyloid status (based on Centiloid cut-point <12 measured by PET-CT)
  • APOEe4 negative status
  • Willingness to participate in exercise interventions

Exclusion criteria

  • Pathological diagnosis related to physical or mental condition
  • No living in community settings during the study
  • MRI incompatibility
  • Ambulatory with pain or regular use of an assisted walking device
  • Severe cardiovascular or respiratory conditions
  • Participation in another clinical trial within the last 30 days

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

20 participants in 3 patient groups

Aerobic exercise group
Experimental group
Description:
-Aerobic group. 30 min at 60-70% of the Maximal Heart Rate, moderate intensity on cycle.
Treatment:
Behavioral: Aerobic exercise condition
Resistance exercise group
Experimental group
Description:
30 min at 4-6 RPE (OMNI-Resistance Exercise Scale of Perceived Exertion), 3 sets of 8 exercise/set, 40 sec/exercise. Moderate intensity using elastic bands and body weight.
Treatment:
Behavioral: Resistance exercise condition
Control
No Intervention group
Description:
30 min seated watching a neutral documentary without cognitive engagement

Trial documents
2

Trial contacts and locations

2

Loading...

Central trial contact

Irene Esteban-Cornejo, RYC Asistance Professor, PhD; Francisco B Ortega, Professor

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems