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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02708485
Other study ID # 09-043
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 2009
Est. completion date July 2017

Study information

Verified date July 2017
Source Université de Sherbrooke
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to evaluate the effect of a 3-month walking program on brain energy metabolism in patient with mild Alzheimer's disease (AD). Two groups of sedentary patients with mild AD are followed and compared over a 3-month period of time: Control (non-active) and walking (from 15 to 45 minutes of exercise on a treadmill, 3 times a week for 12 weeks) groups. All the participants are evaluated on their cognition, brain volumes (MRI) and brain fuel consumption (PET scan with 18-FDG and 11C-AcAc) at the beginning and at the end of the study.


Recruitment information / eligibility

Status Completed
Enrollment 15
Est. completion date July 2017
Est. primary completion date July 2017
Accepts healthy volunteers No
Gender All
Age group 40 Years and older
Eligibility Inclusion Criteria:

- Diagnosis of mild Alzheimer's disease (NINCDS-ADRDA criteria)

- Taking cholinesterase inhibitors

- Sedentary

- Ability to do physical exercise

Exclusion Criteria:

- Parkinson disease

- Down syndrome

- Epilepsy or concussion

- Drug or alcohol abuse

- Past psychiatric history

- Vitamin B12 Deficiency

- Uncontrolled diabetes or thyroid function

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Physical exercise
A 3-month walking program (3 times a week for 12 weeks) on treadmill supervised by a physiotherapist. Duration of the exercise is progressively increased from 15 min to 45 min over a 6-week period and the intensity of the exercise is moderate (a 12-13 score on Borg scale).

Locations

Country Name City State
Canada Research Centre on Aging (CSSS-IUGS - CIUSSS de l'Estrie - CHUS) Sherbrooke Quebec

Sponsors (1)

Lead Sponsor Collaborator
Université de Sherbrooke

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Brain Glucose Consumption Brain glucose uptake (umol/100g/min) using 18F-FDG PET imaging 3 months
Primary Brain Acetoacetate Consumption Brain acetoacetate uptake (umol/100g/min) using 11C-AcAc PET imaging 3 months
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