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Physical ActivityDEACSNCT07710339

Ecological Momentary Cognitive Assessment

A study testing Exercise and Daylong Movement in people with Physical Activity and Cognition, run by Wake Forest University at 1 site in United States.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

The purpose of this study is to characterize the relationships between changes in cognitive functioning across the day and patterns of physical activity in older adults. Those who participate in the program will complete tests of cognition and several surveys at the start. Read more about this study

Who is it for?
Ages 65 years and olderHealthy volunteers can take part
Conditions the study is for
Physical Activity, Cognition, Aging
What is being tested?
Exercise and Daylong Movement
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteUnited States
Study dates
15 Aug 2026to 1 Apr 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

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 65 years and older
  • All sexes
  • Healthy volunteers accepted
  • Older adult

Who may be able to join

  • age ≥65
  • fluent in English
  • own a smartphone
  • able to provide digital informed consent
  • able to walk without assistance from others (a cane or walker is allowed)
  • low-active as defined by participating in purposeful aerobic exercise two days or less per week

Who cannot join

  • potential neurological cofounders (stroke, seizure disorder, recent head injury or loss of consciousness)
  • diagnosis of clinical mental abnormalities (e.g., schizophrenia, bipolar disorder, Parkinson's Disease, Alzheimer's disease and related dementias)
  • any other conditions that may impact their ability to complete the ecological momentary cognitive tasks or physical activity (e.g., visual or auditory impairments, uncontrolled arthritis)
  • A score lower than 32 on the TICS-M.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Carter Stoke, BS contact

336-758-5042

stokcm25@wfu.edu

United States1 site
  • Health and Exercise Sciences

    Winstom Salem, North Carolina, 27109

    Jason Fanning, PhD, 336-758-5042, fanninjt@wfu.edu

Other trials in United States

About this study

Official title: Characterizing Daily Activity and Cognition in Older Adults

The purpose of this study is to characterize the relationships between changes in cognitive functioning across the day and patterns of physical activity in older adults. Those who participate in the program will complete tests of cognition and several surveys at the start. They will then wear an activity monitor and complete four cognitive tests plus surveys per day for one week. After this week concludes, they will continue completing the surveys and cognitive tests, and will engage in one week of structured exercise at a research center and one week where they work to move throughout the day.

Being tested
Exercise, Daylong Movement
Medical subject headings
Motor Activity

What participants receive

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

  • ExerciseBehavioural

    During this week, participants will be encouraged to complete 5 supervised center-based aerobic exercise sessions at a moderate to vigorous intensity.

  • Daylong MovementBehavioural

    Participants will work to increase daily steps by approximately 25% while avoiding sustained periods of sitting.

Study groups in NCT07710339
Study groupRoleWhat they receive
Control-Exercise FirstExperimentalThis condition completes the control week followed by structured exercise and then moving throughout the day.
Receives: Behavioral: Exercise; Behavioral: Daylong Movement
Control-Daylong Movement FirstExperimentalThis condition completes the control week followed by moving throughout the day and then exercise.
Receives: Behavioral: Exercise; Behavioral: Daylong Movement

What is being measured

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

  1. Daily cognitive performance

    Average performance on ecological momentary cognitive tasks, completed up to 4 times daily: color trick (inhibition), 2-back (working memory), hand swype (task switching)

    Measured: From start of control week to the end of participation at 3 weeks.

Timeline

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

  1. First posted17 Jul 2026
  2. Study start15 Aug 2026 (estimated)
  3. Primary completion1 Apr 2027 (estimated)
  4. Study completion1 Apr 2027 (estimated)

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
Basic science
Allocation
Randomised
Intervention model
Crossover
Model description
Participants complete one "control" week and then are randomly assigned to begin with either exercise or moving across the day before engaging in the remaining intervention arm.
Masking
None (open label)
Enrolment
30 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07710339
Sponsor's protocol ID
IRB00026492
Acronym
DEACS
Status last verified
Jul 2026
First submitted
13 Jul 2026
Last updated
17 Jul 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Exercise and Daylong Movement in people with Physical Activity and Cognition, run by Wake Forest University at 1 site in United States.

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 6 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: opening soon, as of the sponsor's last update on 17 Jul 2026. 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 United States. 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?

This study is still under way. Results are not available in the source record yet.

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

Contact Carter Stoke, BS (336-758-5042, stokcm25@wfu.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Daily cognitive performance (time frame: From start of control week to the end of participation at 3 weeks.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 17 Jul 2026.

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