The Effects of an Extensive Exercise Program on the Progression of Mild Cognitive Impairment

NCT02913053 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 183

Last updated 2019-11-14

No results posted yet for this study

Summary

Exercise interventions to prevent dementia and delay cognitive decline have gained considerable attention in recent years. Human and animal studies have demonstrated that regular physical activity targets brain function by increasing cognitive reserve. Although initial studies indicate enhanced cognitive performance in patients with mild cognitive impairment (MCI) following an exercise intervention, little is known about the effect of an extensive, controlled and regular exercise regimen on the neuropathology of patients with MCI.

The aim of this study is to compare a 12- month aerobic exercise programme versus a stretching and toning (non-aerobic) programme versus a control group on the progression of cognitive decline in MCI.

It is hypothesized that MCI-related decreases in cognitive and psychomotor functioning will show less progression or even be improved after a one-year aerobic exercise intervention compared to a group of patients undergoing stretching and toning exercise as well as to a control group provided with no intervention.

Conditions

Interventions

BEHAVIORAL

Aerobic exercise

Patients with mild cognitive impairment will undergo a one-year aerobic exercise program of 3 units of 45 min / week

BEHAVIORAL

Non-aerobic exercise

Patients with mild cognitive impairment will undergo a one-year stretching and toning (non-aerobic) exercise program of 3 units of 45 min / week

Sponsors & Collaborators

  • German Sport University, Cologne

    collaborator OTHER
  • University of Dublin, Trinity College

    collaborator OTHER
  • University of Bonn

    collaborator OTHER
  • University Hospital, Bonn

    collaborator OTHER
  • Radboud University Medical Center

    lead OTHER

Principal Investigators

  • Stefan Schneider, Prof · German Sport University, Germany

  • Brian Lawlor, Prof · Trinity College Dublin, Ireland

  • Marcel Olde Rikkert, Prof · Radboud University, Netherlands

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-06-30
Primary Completion
2018-11-30
Completion
2018-12-31

Countries

  • Germany
  • Ireland
  • Netherlands

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02913053 on ClinicalTrials.gov