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A Combined Training Program for Veterans With Amnestic Mild Cognitive Impairment

Not Applicable
Completed
Conditions
Amnestic Mild Cognitive Impairment
Interventions
Behavioral: Combined Aerobic and Resistance Exercise
Behavioral: Stretching Exercises
Behavioral: Cognitive Training
Registration Number
NCT01962038
Lead Sponsor
Palo Alto Veterans Institute for Research
Brief 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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
72
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

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Stretching Exercises/Cognitive TrainingCognitive Training-
Combined Aerobic and Resistance Exercise/Cognitive TrainingCombined Aerobic and Resistance Exercise-
Combined Aerobic and Resistance Exercise/Cognitive TrainingCognitive Training-
Stretching Exercises/Cognitive TrainingStretching Exercises-
Primary Outcome Measures
NameTimeMethod
Change from Baseline to 28 weeks in delayed recall of a word listBaseline, 24 weeks, 28 weeks
Change from Baseline to 28 weeks in Delayed Recall of Names-Face TaskBaseline, 24 weeks, 28 weeks
Secondary Outcome Measures
NameTimeMethod
Non-Cognitive Outcomes (Depression, Sleep, Quality of Life)Baseline, Time 2, Time 3

Trial Locations

Locations (1)

VA Palo Alto Health Care System

🇺🇸

Palo Alto, California, United States

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