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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01962038
Other study ID # FAI0002AGG
Secondary ID
Status Completed
Phase N/A
First received August 26, 2013
Last updated April 3, 2018
Start date May 2013
Est. completion date November 2017

Study information

Verified date April 2018
Source Palo Alto Veterans Institute for Research
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is examine the efficacy of a combination physical exercise and cognitive training program on improving memory in older Veterans with amnestic Mild Cognitive Impairment.


Recruitment information / eligibility

Status Completed
Enrollment 72
Est. completion date November 2017
Est. primary completion date July 2017
Accepts healthy volunteers No
Gender All
Age group 50 Years to 90 Years
Eligibility Inclusion Criteria:

- diagnosis of amnestic Mild Cognitive Impairment

- available informant

- visual and auditory acuity to allow neuropsychological testing

- willingness to participate in exercise training + cognitive training for 8 months

- approval of primary provider to participate in exercise trial

Exclusion Criteria:

- current severe psychiatric disorder

- diagnosis of dementia

- history of neurological or system illness affecting CNS function

- acute illness or unstable chronic illness

- current severe cardiac disease

- inability to exercise consistently because of orthopedic or musculoskeletal problems

- morbid obesity

- inability to read, verbalize understanding and voluntarily sign the informed consent

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Combined Aerobic and Resistance Exercise
Gym and home based aerobic and resistance exercises
Stretching Exercises
Gym and home based stretching exercises
Cognitive Training
Group-based cognitive training

Locations

Country Name City State
United States VA Palo Alto Health Care System Palo Alto California

Sponsors (2)

Lead Sponsor Collaborator
Palo Alto Veterans Institute for Research U.S. Army Medical Research and Materiel Command

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Exercise Assessment Baseline, Time 2, and Time 3
Primary Change from Baseline to 28 weeks in delayed recall of a word list Baseline, 24 weeks, 28 weeks
Primary Change from Baseline to 28 weeks in Delayed Recall of Names-Face Task Baseline, 24 weeks, 28 weeks
Secondary Non-Cognitive Outcomes (Depression, Sleep, Quality of Life) Baseline, Time 2, Time 3
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