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Physical Activity and Cognition Study

Feasibility of Using Physical Activity Monitoring for Enhancing Cognition in Healthy Seniors

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02773121
Acronym
CTSI
Enrollment
28
Registered
2016-05-16
Start date
2017-03-01
Completion date
2020-01-17
Last updated
2020-04-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aging

Keywords

Cognition, Learning, Memory, Executive Function, Attention, Neuropsychological Tests, Physical Activity, Physical Fitness, Exercise, Resistance Training, Walking, Muscle Stretching Exercises, Exercise Test, Balance, Flexibility, Body Composition

Brief summary

The goal of this research study is to examine whether an intervention to increase physical activity using a body-worn sensor affects cognitive (thinking) processes.

Detailed description

The overall duration of participation in this research study is approximately 4 months. During this time, three study visits will be required. The first visit is for informed consent and screening, the second visit is for baseline fitness and cognitive testing, and the third visit is for follow-up fitness and cognitive testing after a 12-week physical activity monitoring program. Participants will be randomized to one of two study arms, a physical activity monitoring arm and a flexibility and balance arm. Both study arms involve wearing a physical activity sensor and monitoring physical activity for a duration of 12 weeks.

Interventions

BEHAVIORALPhysical Activity

Trainer-guided at-home behavioral intervention

Sponsors

Boston University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
55 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* Non-smoking * Age between 55-85 years * Sedentary status (physically inactive; not participating in at least 30 minutes of moderate intensity physical activity on at least three days per week for at least three months) * Generally healthy men and women * Living in the greater Boston area * Available for the 4 month duration of the study * Native-English speaking or fluent in English (must have attended elementary school and higher in English)

Exclusion criteria

* Poor vision that cannot be corrected with glasses or contact lenses * Presence of an acute infection * Diagnosis of kidney failure * Diagnosis of liver disease * Diagnosis of thyrotoxicosis/hyperthyroidism * Diagnosis of cancer * Past or present conditions that affect cognitive functioning: 1. learning disability 2. neurological disorders or conditions (movement disorder, history of head trauma or stroke, epilepsy, etc.) 3. psychiatric disorders or conditions (depression, anxiety disorder, etc.) * Past or present conditions that are counter indicators for participation in cardio-respiratory fitness assessment and moderate-intensity physical activity: 1. heart conditions (e.g. heart attack, arrhythmias, etc.) 2. circulatory conditions (e.g. uncontrolled hypertension, leg claudication, high cholesterol, etc.) 3. respiratory conditions (e.g., asthma or lung conditions, such as chronic obstructive pulmonary disease, acute bronchitis, acute common cold, lung cancer, pneumonia, etc.) 4. current musculoskeletal impairments (e.g. fractures, hemiplegia, chronic joint pain, arthritis, osteoporosis, not able to walk comfortably without assistance, etc.) 5. diagnosis of electrolyte disorder or abnormality 6. presence of diabetes mellitus * Obesity * Prescription medication or other drugs that treat heart, lung, or circulatory conditions (e.g. beta blockers, bronchodilators, etc.) * Prescription medication or other drugs that affect chemicals in the brain (e.g. antidepressants, anxiolytics, etc.) * Implanted medical devices, such as a pacemaker or defibrillator * Unavailable for the approx. 4-month duration of the study

Design outcomes

Primary

MeasureTime frameDescription
Cognition80-90 minutesChange in cognitive task performance post-intervention compared to baseline
Aerobic Fitness30 minutesChange aerobic fitness measured with treadmill test post-intervention

Secondary

MeasureTime frameDescription
Functional fitness: Timed Get Up and Go10 minChange in performance in the Timed Get Up and Go test post-intervention compared to baseline
Functional fitness: Five Times Sit to Stand10 minChange in performance in the Five Times Sit to Stand test post-intervention
Functional fitness: Flexibility10 minChange in performance in the Sit and Reach test post-intervention
Physical activity12 weeksGreater overall moderate-intensity physical activity time and step count and lower sedentary time in the physical activity monitoring than the flexibility and balance group

Other

MeasureTime frameDescription
Gait: stride time variability12 weeksChange in stride time variability over 12 weeks
Gait: step and stride time12 weeksChange in step and stride time over 12 weeks
Gait: gait symmetry12 weeksChange in gait symmetry over 12 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026