Combining Exercise and Cognitive Training to Improve Everyday Function (EXACT)

August 29, 2014 updated by: Washington University School of Medicine
The purpose of this randomized, controlled, prospective study is to evaluate the benefits of combining aerobic exercise with cognitive training for optimizing cognitive function. The study will enroll 109 men and women, age 55-75 years who are in stable health and without contraindications to exercise or evidence of dementia or cognitive impairment. Individuals will be randomly assigned to one of four groups for six months: Aerobic Exercise and Health Education, Home Exercise and Cognitive Training, Aerobic Exercise and Cognitive Training, and Home Exercise and Health Education. Participants will undergo measurements of cognitive function, physical performance, and complete questionaires about daily activities, physical activity, and quality of life at baseline (pre-intervention), and at 6 and 12 months after baseline.

Study Overview

Study Type

Interventional

Enrollment (Actual)

96

Phase

  • Phase 3

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Missouri
      • St. Louis, Missouri, United States, 63108
        • Washington University School of Medicine

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

55 years to 75 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • age 55-75 years (inclusive)
  • English-speaking
  • sufficient visual and auditory perception to complete testing
  • available informant (someone who knows the individual well)
  • Clinical Dementia Rating of 0 (non-demented per the screening assessment).

Exclusion Criteria:

  • participation in a regular exercise program in last 6 months
  • participation in a cognitive training program in last 6 months
  • inability to walk on a treadmill or ride an exercise bike
  • less than a 10th grade education
  • mild cognitive impairment or dementia
  • cigarette smoking within the previous year
  • history of alcohol or substance abuse
  • BMI greater than 35
  • insulin-dependent diabetes
  • major and/or unstable medical, neurological, or psychiatric disorder, including:

    • active congestive heart failure
    • unstable angina
    • effort angina
    • nocturnal angina
    • MI within previous 6 months
    • ECG evidence of serious arrhythmias and/or acute myocardial ischemia reflected by ST-segment depression of 0.3 mm
    • resting blood pressure above 170 systolic or 100 diastolic
    • chronic infections
    • advanced arthritis
    • contractures or weakness due to CVA that would prevent adequate performance of the exercises.
    • disabling stroke
    • late stage renal or liver disease
    • major affective disorder with active symptoms

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Factorial Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Combined
Aerobic Exercise + Cognitive Training
Standardized aerobic training program that is individualized to each participant's fitness level, and supervised by a certified exercise specialist. Participants attend 3 training sessions per week for 6 months. The session begins with a 10-15 minute warm-up. Participants then exercise on a treadmill or stationary bike, followed by "cool-down" activities. Heart rate and rating of perceived exertion are used to evaluate exercise intensity. Participants begin at ~30 min/day 60-70% of HR max and/or an equivalent level of RPE, and progress to 45-50 minutes at 75-85% for HR max.
Computer-based training that is is administered 3 days per week for 8 weeks during months 5 and 6. The training program focuses on 3 types of cognitive processes: task coordination, prospective memory, and retrospective memory retrieval. One day of the week is devoted to each of the three cognitive processes. Some training sessions include a homework assignment for application and practice of the target cognitive processes in everyday activities.
Experimental: Exercise
Aerobic Exercise + Health Education
Standardized aerobic training program that is individualized to each participant's fitness level, and supervised by a certified exercise specialist. Participants attend 3 training sessions per week for 6 months. The session begins with a 10-15 minute warm-up. Participants then exercise on a treadmill or stationary bike, followed by "cool-down" activities. Heart rate and rating of perceived exertion are used to evaluate exercise intensity. Participants begin at ~30 min/day 60-70% of HR max and/or an equivalent level of RPE, and progress to 45-50 minutes at 75-85% for HR max.
Weekly educational sessions are administered during months 5 and 6, conducted at the recreational center by research staff. Sessions last 1 hour, and cover health and other topics unrelated to exercise or cognition, such as nutrition, hearing loss, stroke, and saving energy in one's home. At the completion of each session, participants are given a "homework" assignment.
Experimental: Cognitive
Home Exercise + Cognitive Training
Computer-based training that is is administered 3 days per week for 8 weeks during months 5 and 6. The training program focuses on 3 types of cognitive processes: task coordination, prospective memory, and retrospective memory retrieval. One day of the week is devoted to each of the three cognitive processes. Some training sessions include a homework assignment for application and practice of the target cognitive processes in everyday activities.
Exercise program consisting of stretching, range of motion, and simple yoga exercises designed to improve flexibility. Each participant has a 60-minute sessions with an exercise trainer to teach them how to perform the exercises correctly. They are also given diagrams illustrating the exercises, along with written instructions. They are instructed to perform these exercises at home at least 3 times per week for 30 - 45 minutes. They also go to the recreational center monthly to meet with an exercise trainer to ensure that they are doing the exercises correctly. Participants record their exercise activities on a calendar for the 6 months.
Experimental: Control
Home Exercise + Health Education
Weekly educational sessions are administered during months 5 and 6, conducted at the recreational center by research staff. Sessions last 1 hour, and cover health and other topics unrelated to exercise or cognition, such as nutrition, hearing loss, stroke, and saving energy in one's home. At the completion of each session, participants are given a "homework" assignment.
Exercise program consisting of stretching, range of motion, and simple yoga exercises designed to improve flexibility. Each participant has a 60-minute sessions with an exercise trainer to teach them how to perform the exercises correctly. They are also given diagrams illustrating the exercises, along with written instructions. They are instructed to perform these exercises at home at least 3 times per week for 30 - 45 minutes. They also go to the recreational center monthly to meet with an exercise trainer to ensure that they are doing the exercises correctly. Participants record their exercise activities on a calendar for the 6 months.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Memory for Medical Information
Time Frame: Change in memory task performance between baseline and 6 months
This task measures the ability of the individual to learn and recall complex medical information, and the source of the information.
Change in memory task performance between baseline and 6 months
Cooking Breakfast task
Time Frame: Change in task performance between baseline and 6 months
Participants engage in a computerized laboratory simulation of a cooking task to assesses cognitive dimensions of planning, prospective memory, monitoring the progress of ongoing activity, anticipating potential problems, task switching, and task coordination.
Change in task performance between baseline and 6 months
Virtual Week task
Time Frame: Change in task performance between baseline and 6 months
Participants engage a computerized board game that simulates choices about, and recall of, daily and weekly activities.
Change in task performance between baseline and 6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Activities of Daily Living--Yale Physical Activity Scale (YPAS)
Time Frame: Baseline, Month 3, Month 6, Month 12
Questionnaire that objectively measures frequency and time spent per week performing common physical activities, which are used to caculate total weekly metabolic work (KCals).
Baseline, Month 3, Month 6, Month 12
Uniform Data Set (UDS)
Time Frame: Baseline, Month 12
A standardized interview to ascertain and assess demographic information, health status, cognitive status, medications, and functional status. The interview is conducted with the research participant and a collateral source historian.
Baseline, Month 12
Geriatric Depression Scale
Time Frame: Baseline, Month 12
A 15-item questionnaire to assess for symptoms of depression.
Baseline, Month 12
Late Life Function & Disability Index (LLFDI)
Time Frame: Baseline, Month 6, Month 12
A standardized questionnaire to assess performance of activities of daily living (ADLs) and the level of difficulty experienced while performing each activity.
Baseline, Month 6, Month 12
Pittsburgh Sleep Quality Index (PSQI)
Time Frame: Baseline, Month 6, Month 12
Questionnaire to assess sleep quality and events in the prior month. Includes a section for roommate/bed partner response.
Baseline, Month 6, Month 12
Objective Physical Performance Tests
Time Frame: Baseline, Month 6
Physical Performance Test, Senior Fit Test, Dual Task Walking Speed. These tests objectively measure walking speed, muscle strength, balance, and coordination.
Baseline, Month 6
Prospective and Retrospective Memory Questionnaire (PMRQ)
Time Frame: Baseline, Month 6, Month 12
Objective questionnaires to measure ability to learn and recall information.
Baseline, Month 6, Month 12
Peak Aerobic Power
Time Frame: Baseline, Month 6
The participant walks on a treadmill, with a progressively increased grade (level of incline)over a 8-15 minute period, with continuous measurements of expired oxygen and carbon dioxide. Information obtained is used to measure the total amount of work that the person performs during the test. The participant has continuous ECG monitoring during the test.
Baseline, Month 6
Cognitive assessment battery
Time Frame: Baseline, Month 6, Month 12
Array of cognitive tasks to assess performance in a variety of areas. Includes Stroop (response time and attentional control), Trials A/B (sequencing), Crossing Off (motor control), Logical Memory (story recall), and Digit Symbol (corresponding symbols to digits).
Baseline, Month 6, Month 12

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Ellen Binder, MD, Washington University School of Medicine

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

March 1, 2010

Primary Completion (Actual)

August 1, 2012

Study Completion (Actual)

June 1, 2013

Study Registration Dates

First Submitted

May 2, 2012

First Submitted That Met QC Criteria

May 18, 2012

First Posted (Estimate)

May 23, 2012

Study Record Updates

Last Update Posted (Estimate)

September 3, 2014

Last Update Submitted That Met QC Criteria

August 29, 2014

Last Verified

August 1, 2014

More Information

Terms related to this study

Other Study ID Numbers

  • 201102416
  • 1R01AG034581-01 (U.S. NIH Grant/Contract)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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