Activity Tracking, Care Partner Co-participation, Text Reminders, Instructional Education, Video-Guided Physical Rehabilitation, and Exercise
NYU Langone Health · NCT07321587
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 100
- US sites recruiting
- 1
- Study start
- January 26, 2026
- Record last updated
- January 28, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
This is a multi-methods two-arm, crossover, analyst-blinded randomized controlled trial with embedded qualitative interviews, enrolling 50 dyads (older adult-care partner). Participants will receive the ACTIVE intervention, which includes a Fitbit smartwatch, motivational text messages to engage in walking exercise, instructional educational videos, and virtual physical therapy sessions. Intervention components will be delivered over 3 weeks, with continuous monitoring of physical activity via Fitbit data, read receipts of the motivational text messages, and log of engagement in the virtual physical therapy and educational videos.
Being studied: ACTIVE Intervention
Conditions: Mild Dementia
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
Older Adults
- Age ≥65 years.
- With or without mild dementia.
- Willing to consent to participate in the study or have an LAR that is willing to consent for their participation in the study
- Willing to wear a Fitbit smartwatch, receive text messages, watch intervention-related videos, participate in physical therapy, and walking exercise.
- No contraindications to engaging in physical activity.
Care Partners
- Age ≥18 years.
- Met criteria for survey participation.
- Person being cared for is recruited in the study.
- Willing to consent to participation
- Willing to wear a Fitbit smartwatch, receive text messages, watch intervention-related videos, participate in physical therapy, and walking exercise.
- No contraindications to engaging in physical activity.
Exclusion Criteria
Older Adults
- Severe cardiac, neurologic, or musculoskeletal condition (including but not limited to recent or untreated fracture in any part of the body)
- limiting participation in daily walking or Fitbit smartwatch use.
- Moderate to severe dementia (using the clinical dementia rating scale of 2 or higher
- Inability to operate or manage a Fitbit smartwatch device (even with care partner support).
- No phone or phone not capable of receiving text messages or watching videos.
- No internet for watching videos
Care Partners
- Severe cardiac, neurologic, or musculoskeletal condition limiting participation in daily walking or Fitbit smartwatch use.
- Pregnant care partners
- Any level of dementia or cognitive impairment among care partners
- Inability to operate or manage a Fitbit smartwatch device.
- Inability to co-participate in intervention tasks with older adult
- No phone or phone not capable of receiving text messages or watching videos.
- No internet for watching videos
Recruiting US locations
NYU Langone Health
New York, NY 10016
Study contacts (from the official record)
- Oluwaseun Adeyemi, MD, PhD · 980-939-9764 · Oluwaseun.Adeyemi@nyulangone.org
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