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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00629174
Other study ID # 28_12_2005
Secondary ID
Status Recruiting
Phase Phase 3
First received February 25, 2008
Last updated March 11, 2008
Start date June 2006

Study information

Verified date March 2008
Source Charite University, Berlin, Germany
Contact Fernando Dimeo, MD
Phone +49308445
Email fernando.dimeo@charite.de
Is FDA regulated No
Health authority Germany: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The trial will evaluate the effects of frequent exercise and increased mental activity on the age-related impairment of cognitive function in elderly women. Furthermore, we will assess the effects of exercise and mental activity on the mood, physical performance and mental status of participants. We will also search for genetic factors which may be responsible of the observed outcomes.


Description:

Two-hundred and fifty-two women older than 70 years will be randomize to one of three groups. The first (exercise) will participate at an exercise program three times weekly for 90 minutes. The training will consist of an endurance and resistance training and will be carried out in a group. Participants in the second group (mental training) will take computer lessons, three times weekly for 90 minutes. Both interventions will be carried out for 26 weeks. Participants in the third group (control) will not participate at an structured intervention.


Recruitment information / eligibility

Status Recruiting
Enrollment 252
Est. completion date
Est. primary completion date December 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 70 Years and older
Eligibility Inclusion Criteria:

- All healthy women older than 70 years with sufficient knowledge of German can participate.

Exclusion Criteria:

- Chronic mental disorders

- Chronic neurological, cardiological, pulmonary or renal diseases.

- Severe osteoarthritis

- Disorders which can be aggravated by exercise (arterial hypertension, coronary heart disease, COLD).

- Cancer in current therapy

- Treatment with glucocorticoids or cytostatic drugs.

- Patients who received an organ transplantation

- Exercise-induced osteoarticular pain

Study Design

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


Related Conditions & MeSH terms


Intervention

Behavioral:
Exercise
Endurance and resistence training, 90 minutes, 3 times weekly
Mental activity
Participation at computer lessons, 3 times weekly, 90 minutes each

Locations

Country Name City State
Germany Department of Psychiatry Berlin
Germany Section Sports Medicine, Charité - Universitätsmedizin Berlin Berlin

Sponsors (3)

Lead Sponsor Collaborator
Charite University, Berlin, Germany German Research Foundation, Gertrude and Hugo Adler Foundation

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Improvement of cognitive and physical performance 6 months No
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