Telehealth-Adapted Compensatory Training and Intervention for Cognition (NCT07366346)
Telehealth-Adapted Compensatory Training and Intervention for Cognition for People With Mild Cognitive Impairment
🩺 Plain-English Summary (8th-Grade Level)
The goal of this clinical trial is to develop a five-week virtual cognitive training intervention for people with Mild Cognitive Impairment (MCI) based off an existing eight-week intervention. The main question it aims to answer is: • Is five weeks of training as good as eight weeks in improving cognition, quality of life, daily functioning, and mood, and in reducing caregiver burden? Researchers will compare five weeks of cognitive training to eight weeks of training to see if the shorter version is as effective as the full training. Participants will complete all activities virtually: * Complete a screening visit with a study partner (typically a family member, roommate, or close friend) to determine eligibility to participate in the study * Complete some tests of memory and thinking and some questionnaires * Attend weekly two-hour group cognitive training sessions with a trained group leader, for five or eight weeks * Redo the questionnaires and tests of memory and thinking immediately after completing the training, and three months after completing the training
Who can join: Review the eligibility criteria below.
Location: University of Florida — Gainesville, Florida
Age range: 65 Years to 84 Years
🧪 Interventions in This Study
- Motivationally Enhanced Compensatory Cognitive Training for Mild Cognitive Impairment (ME-CCT-MCI) (BEHAVIORAL)
- Brief Motivationally Enhanced Compensatory Cognitive Training for Mild Cognitive Impairment (bME-CCT-MCI) (BEHAVIORAL)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (1 Sites)
- University of Florida — Gainesville, Florida
📞 Contact the Study Coordinator
Phone: (352) 294-8765
Email: c.perrin@phhp.ufl.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in MCI
- Studying the Effects of Digital Interventions on Cognition, Wellbeing, Stress, and Sleep in Older Adults — San Francisco, California
- Personalized Closed-Loop Brain Stimulation for Patients With Mild Cognitive Impairment — Baltimore, Maryland
- Cognitive-Motor Training for AD/ADRD Prevention — Chicago, Illinois
- FACE Phase II (a Stage II Trial) — Palo Alto, California
Explore by condition: All MCI clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.