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Mild Cognitive ImpairmentNCT00958867

EXCEL: Exercise for Cognition and Everyday Living for Seniors With Memory Complaints

A study testing Exercise program (AT) and Exercise training (RT) in people with Mild Cognitive Impairment, run by University of British Columbia at 1 site in Canada.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Alzheimer's disease (AD) is a major health issue in Canada; it affects over 8% of the population aged over 65 years. Persons with AD have a reduced quality of life as they become dependent on others for activities of daily living (ADLs). Read more about this study

Who is it for?
Ages 70 years and older, women onlyHealthy volunteers can take part
Conditions the study is for
Mild Cognitive Impairment
What is being tested?
Exercise program (AT) and Exercise training (RT)
Could I receive a placebo?
No, everyone receives an active treatment
How many people
86 participants
Where
1 siteCanada
Study dates
Aug 2009to Mar 2010
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 70 years and older
  • Women only
  • Healthy volunteers accepted
  • Older adult

Who may be able to join

  • Community-dwelling senior women;
  • Aged 70 years and older;
  • Subjective memory complaints as determined by interview;
  • MMSE score > 24/30;
  • Scored < 26/30 on the MoCA (74);
  • Visual acuity of at least 20/40, with or without corrective lenses; and
  • Physician approval for participation in an exercise program.

Who cannot join

  • Diagnosed neurodegenerative disease (e.g., AD) and a history of stroke;
  • Have clinically significant peripheral neuropathy or severe musculoskeletal or joint disease;
  • Diagnosed with a psychiatric condition; or
  • Diagnosed with dementia of any type.

Trial locations and contacts

1 site in 1 country.

Canada1 site
  • Centre for Hip Health Mobility

    Vancouver, British Columbia

Other trials in Canada

About this study

Official title: Enhancing Cognition and Functional Independence in Senior Women With Mild Cognitive Impairment: A Randomized Trial of Aerobic vs. Resistance Training

Alzheimer's disease (AD) is a major health issue in Canada; it affects over 8% of the population aged over 65 years. Persons with AD have a reduced quality of life as they become dependent on others for activities of daily living (ADLs). This problem of loss of independence - functional dependence - is one focus of this grant application. It is projected that by 2020, Canada will have well over 10 million seniors with moderate to severe functional dependence. Functional dependence was the most significant contributor to an annual cost of dementia that had already reached $4 billion in the 1990s.

Mild cognitive impairment (MCI) is a well-recognized risk factor for both AD and functional dependence. Within the broader assessment of cognitive function, the literature suggests that executive functioning - the ability to concentrate, to attend selectively, to plan and strategize - is a robust cognitive predictor of functional status in seniors. Specifically, Royall and colleagues demonstrated executive functioning independently explained 43% of the functional status in community-dwelling seniors dementia. The researchers will investigate executive functioning in seniors with MCI.

Read more

Randomized trials of various exercise interventions have proven that exercise has many systemic benefits. Data are emerging that physical activity may improve cognition - specifically executive function - in healthy adults. The researchers' own pilot data suggest that resistance training in seniors may improve executive functioning as assessed by neuropsychological tests and neuro-imaging. However, at present the Cochrane Database of Systematic Reviews indicates there are insufficient published data to guide exercise prescription to prevent AD. In persons with MCI, no published studies have reported on whether physical activity can improve executive function, or delay its decline and thus, prevent or delay the onset of functional dependence (and later, dementia).

Therefore, among seniors with MCI, the researchers will investigate whether or not specific exercise prescription can: 1) provide absolute or relative improvement in cognitive function, particularly executive function; and 2) help maintain functional independence. This will facilitate the development of effective exercise-based strategies for the prevention of both cognitive and functional decline in the large population of seniors with MCI - people at greatly increased risk for AD.

The researchers' proposed research aims to ascertain whether a six-month, twice-weekly aerobic training (AT) program and a six-month, twice-weekly resistance training (RT) program, compared with a six-month, twice-weekly stretch \& relax (S \& R; control) program, will significantly improve cognition and functional status in community-dwelling women with MCI aged 70 years and older.

Primary Hypothesis:

At the end of six-month randomized trial, compared with the S \& R program, both the AT and RT programs will significantly improve cognitive performance, as assessed by neuropsychological testing.

Secondary Hypotheses:

At the end of the six-month randomized trial, compared with the S \& R program, participants of the AT and RT programs will:

  1. Demonstrate evidence of cortical plasticity by fMRI, such as increased activation in cortical regions responsible for item and relational memory; and
  2. Will significantly improve their everyday problem solving ability.
Read the detailed description

STUDY DESIGN, TRIAL PROFILE, AND TIMELINE To achieve our research objectives, we will conduct a six-month, single-blinded (assessors), randomized trial. 75 community-dwelling older women with MCI will be randomly assigned to one of three experimental groups: 1) RT; 2) AT; or 3) S \& R (Control). The study sample is restricted to women as the magnitude of response in cognition to exercise differs between sexes.

METHODS Recruitment We will recruit seniors who are interested in a study of exercise and cognition through media such as newspaper ads, flyers, and posters in community and senior centres. Interested individuals be screened. The screening session will include the following: 1) MMSE ; 2) Montreal Cognitive Assessment (MoCA) ; and 4) Lawton and Brody Instrumental Activities of Daily Living Scale. Individual who meet the inclusion criteria will be invited to join the research study.

Inclusion Criteria

  1. Community-dwelling senior women as the female to male ratio for dementia is 2:1;
  2. Aged 70 years and older;
  3. Subjective memory complaints as determined by interview;
  4. MMSE score > 24;
  5. Scored < 26 on the MoCA;
  6. Visual acuity of at least 20/40, with or without corrective lenses; and
  7. Physician approval for participation in an exercise program. Exclusion Criteria
  8. Diagnosed neurodegenerative disease (e.g., AD) and stroke; 2) Have clinically significant peripheral neuropathy or severe musculoskeletal or joint disease; 3) Diagnosed with a psychiatric condition; 4) Previously diagnosed with dementia of any type; Measurements We have extensive experience in using each of the following methods and instruments. All measures, unless otherwise indicated, will be assessed at each measurement session.

General Screen and Descriptors (90 mins)

  1. General Health and Socioeconomic Status: General health and socioeconomic status will be ascertained by a questionnaire.
  2. Global Cognitive Function and Depression: Global cognitive function will be assessed using the MMSE. The Beck's Depression Inventory (BDI) will be administered. MCI Screen: There are no consensus criteria for the clinical classification of MCI. The MoCA will be used to screen participants for MCI. The MoCA is a brief screening tool for MCI with high sensitivity and specificity. It is a 30-point test covering eight cognitive domains and scores below 26 are considered to be abnormal. A bonus point is given to those with less than 12 years of education.
  3. Physical Activity Level: Physical activity, not including the study-assigned exercise classes, will be determined at baseline and throughout the six-month study period. We will administer the valid and reliable Physical Activities Scale for the Elderly (PASE) questionnaire monthly. Designed for those aged 65 years and older, participants use a 12-item scale to self-report the average number of hours per day spent participating in leisure, household, and occupational physical activities over the previous seven-day period.
  4. IADLs: Participants will complete the Lawton and Brody Instrumental Activities of Daily Living Scale to screen for impaired IADLs. This scale subjectively assesses ability to telephone, shopping, food preparation, housekeeping, laundry, mode of transportation, responsibility for own medication, and ability to handle finances.

Cognitive Performance Measures:

Memory:

We will assess item and relational memory using a computerized paradigm. We will also assess spatial memory and working memory (i.e., N-1 back) using computer paradigms. In all computer paradigms, we will record reaction time and accuracy. We will use the RAVLT to assess verbal memory.

Executive Functions:

We will assess three executive functions: 1) set shifting using the Trail Making Test (Part B) and a computerized paradigm of dual-task; 2) updating (i.e., working memory) using the verbal digits backward test and a computerized paradigm of N-back; and 3) response inhibition using the Stroop Colour-Word Test.

Cortical Activation (60 mins): To accurately assess the effect of both AT and RT on cortical plasticity, we will collect pre- and post-intervention fMRI data from all participants (i.e., AT, RT, and S \& R).

Muscular Strength: We will assess dominant quadriceps (isometric) strength by strain gauge to the nearest 0.5 kilogram.

Six-Minute Walk (6 MWT): This is a walking test of physical status to assess general cardiovascular capacity in seniors 19. The total distance walked in meters in six minutes is recorded.

Balance and Mobility: General balance and mobility will be assessed with the National Institute on Aging (NIA) Balance Scale.

Everyday Problem Solving Ability will be assessed using Everyday Problems Test (EPT). The EPT is a research and assessment tool for measuring adults' ability to solve tasks of daily living that involve printed material. The focus of the measure is on assessing the adults' cognitive competence to reason and solve problems associated with daily living.

Randomization After baseline measurement, participants will be randomized by computer generated random draw to one of the three experimental groups (AT, RT, and S \& R) using www.randomization.com.

Exercise Programs Resistance Training: The protocol for the RT program will be progressive and high-intensity with the aim of increasing muscle strength in the extremities and the trunk. Both a Keiser® Pressurized Air system (Keiser Corp.CA, US) and free weights will be used to provide the training stimulus. Participants will undergo a two-week familiarisation period with the equipment and the exercises. The exercises will consist of biceps curls, triceps extension, seated row, latissimus dorsi pull downs, mini-squats, mini-lunges, hamstring curls, and calf raises. The intensity of the training stimulus will initially be at 50% to 60% of 1 repetition maximum (RM) as determined at week two, with a work range of two sets of 10-15 repetitions and progress to 75% to 85% of 1RM at a work range of six to eight repetitions (two sets) by week four. The training stimulus will be increased using the 7RM method, when two sets of 6-8 repetitions are completed with proper form and without discomfort. Squats and lunges will be performed initially with body weight; loading will be increased only when proper form is maintained for two sets of 10 repetitions. The number of sets completed and the load lifted for each exercise will be recorded for each participant at every class.

Cardiovascular Training: The AT program will be an outdoor walking program. We will use three techniques to monitor exercise intensity. Each participant will: 1) wear a heart rate monitor and will be asked to work at 65% to 80% of her age specific target heart rate; 2) subjectively monitor the intensity of each workout using the Rating of Perceived Exertion.

Stretch and Relax (Control): The S \&R program will consist of stretching exercises, deep breathing, and relaxation techniques. There is no evidence that these exercises improve cognitive function. This group will serve to control for confounding variables such as physical training received by traveling to the community centre for twice-weekly classes, social interaction, and changes in lifestyle secondary to study participation.

Being tested
Exercise program (AT), Exercise training (RT), Exercise training (S & R; control)
Keywords
Resistance exercise training, aerobic exercise training
Medical subject headings
Cognitive Dysfunction

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Exercise program (AT)Behavioural

    Six-month, twice-weekly aerobic training (AT) program

  • Exercise training (RT)Behavioural

    Six-month, twice-weekly resistance training (RT) program

  • Exercise training (S & R; control)Behavioural

    Six-month, twice-weekly stretch \& relax (S \& R; control) program

Study groups in NCT00958867
Study groupRoleWhat they receive
1ExperimentalSix-month, twice-weekly aerobic training (AT) program
Receives: Behavioral: Exercise program (AT)
2ExperimentalSix-month, twice-weekly resistance training (RT) program
Receives: Behavioral: Exercise training (RT)
3Active comparatorSix-month, twice-weekly stretch \& relax (S \& R; control) program
Receives: Behavioral: Exercise training (S & R; control)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Cognitive performance after 3 and 6 months of training

    Measured: 6 months

Secondary outcomes (1)
  1. Everyday problem-solving ability after 3 and 6 months of exercise training, brain function after 6 months of training and physical function after 3 and 6 months of training

    Measured: 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted13 Aug 2009 (estimated)
  2. Study startAug 2009
  3. Primary completionAug 2009
  4. Study completionMar 2010

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Single group
Masking
Single blind
Who is masked
Participant
Enrolment
86 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00958867
Sponsor's protocol ID
H09-00365
Status last verified
Oct 2017
First submitted
11 Aug 2009
Last updated
4 Oct 2017
Results posted
No
Data monitoring committee
Yes

Publications

  • ten Brinke LF, Bolandzadeh N, Nagamatsu LS, Hsu CL, Davis JC, Miran-Khan K, Liu-Ambrose T. Aerobic exercise increases hippocampal volume in older women with probable mild cognitive impairment: a 6-month randomised controlled trial. Br J Sports Med. 2015 Feb;49(4):248-54. doi: 10.1136/bjsports-2013-093184. Epub 2014 Apr 7.

    PubMed 24711660
  • Davis JC, Bryan S, Marra CA, Sharma D, Chan A, Beattie BL, Graf P, Liu-Ambrose T. An economic evaluation of resistance training and aerobic training versus balance and toning exercises in older adults with mild cognitive impairment. PLoS One. 2013 May 14;8(5):e63031. doi: 10.1371/journal.pone.0063031. Print 2013.

    PubMed 23690976

Questions about this trial

What is this clinical trial studying?

A study testing Exercise program (AT) and Exercise training (RT) in people with Mild Cognitive Impairment, run by University of British Columbia at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 4 Oct 2017. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Cognitive performance after 3 and 6 months of training (time frame: 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00958867, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Oct 2017.

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