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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01475396
Other study ID # Exercise_Neuromod
Secondary ID
Status Active, not recruiting
Phase Phase 3
First received November 7, 2011
Last updated June 18, 2012
Start date March 2006
Est. completion date December 2012

Study information

Verified date June 2012
Source University Hospital Muenster
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Interventional

Clinical Trial Summary

Physical activity is thought to increase overall body functions and to decrease cardiovascular and stroke risk factors. Now the question arose, wether enhanced exercise could also exert positive influence on cognition in the aging brain. Therefore, 50 to 80 years old healthy subjects take part in a prospective study with regular sports activity during 6 months. Cognitive functions are detected with sensitive neuropsychological outcome measures, further investigations include MRT of the head, lactat- and other physical measures as well as detailed serum profiles. As a hypothesis, enhanced physical activity is suggested to predict better cognitive performance.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 120
Est. completion date December 2012
Est. primary completion date March 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 50 Years to 80 Years
Eligibility Inclusion Criteria:

- 50-80 years old

- healthy

- lesser activity

Exclusion Criteria:

- regular physical activity

- diabetes

- stroke

- heavy smoking, drinking,

- BMI < 20

- MMSE < 25

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Behavioral:
exercise


Locations

Country Name City State
Germany University Hospital of Muenster Muenster NRW

Sponsors (2)

Lead Sponsor Collaborator
University Hospital Muenster German Federal Ministry of Education and Research

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change of reaction times in ms in a motor learning task after 6 months of intervention/control condition 6 months No
Primary Change of delayed memory scores in #of words in a Verbal learning task after 6 months of intervention/control condition 6 months No
Primary Change of performance in ms in a reaction time task after 6 months of intervention/control condition 6 months No
Primary Change of relative regional grey matter volumes in % measured by T1-weighted MRI after 6 months of intervention/control condition 6 months No
Secondary Change of physical measurements (ECG)/fitness assessments (lactate) after 6 months of intervention/control condition 6 months No
Secondary Change of BDNF blood serum levels in ng/dl after 6 months of intervention/control condition 6 months No
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