Physical Activity and Cognition Study

Not Applicable

Completed

• Conditions: Aging

• Registration Number: NCT02773121
• Lead Sponsor: Boston University

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.

Study Timeline

• Study First Submitted: 2016-05-11
• Study First Submitted QC: 2016-05-12
• Study First Posted: 2016-05-16
• Study Start: 2017-03-01
• Primary Completion: 2020-01-17
• Study Completion: 2020-01-17
• Status Verified: 2020-04
• Last Update Submitted: 2020-04-19
• Last Update Posted: 2020-04-21

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 28

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Cognition	80-90 minutes	Change in cognitive task performance post-intervention compared to baseline
Aerobic Fitness	30 minutes	Change aerobic fitness measured with treadmill test post-intervention

Secondary Outcome Measures

Name	Time	Method
Functional fitness: Five Times Sit to Stand	10 min	Change in performance in the Five Times Sit to Stand test post-intervention
Functional fitness: Timed Get Up and Go	10 min	Change in performance in the Timed Get Up and Go test post-intervention compared to baseline
Functional fitness: Flexibility	10 min	Change in performance in the Sit and Reach test post-intervention
Physical activity	12 weeks	Greater overall moderate-intensity physical activity time and step count and lower sedentary time in the physical activity monitoring than the flexibility and balance group

Trial Locations

Locations (1)

Boston University School of Medicine; 🇺🇸 Boston, Massachusetts, United States