COPD Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have a documented diagnosis of a complicated-mild, moderate, or severe traumatic brain injury (TBI), confirmed through records such as emergency services reports, hospital records, or doctor's notes, and who required a stay in an inpatient rehabilitation unit
- People who are at least 12 months past the date of their brain injury
- People who have access to the internet through a computer, tablet, or smartphone
- People who can speak and understand English or Spanish
- People who are willing to take part in the study
- People who have been cleared to participate by a doctor or recognized health professional, such as a primary care physician, specialist, or rehabilitation therapist
Who may not be able to join:
- People who do not have a history of complicated-mild, moderate, or severe traumatic brain injury
- People who are fewer than 12 months past their brain injury
- People who are currently in a minimally conscious or vegetative state
- People who are starting a new treatment — such as physical therapy, occupational therapy, vestibular therapy, psychotherapy, or a new medication — at the time the study begins, if the principal investigator or medical monitor believes it could affect the study results (people whose treatments have been stable may still be eligible — confirm with trial site)
- People who, in the judgment of the study team, have significant cognitive difficulties such as delirium or dementia that would prevent them from meaningfully consenting to or participating in the study
- People who, in the judgment of the study team, have a serious or major disabling medical condition that would prevent them from meaningfully consenting to or participating in the study
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Tamara Bushnik, PhD, NYU Langone Health
Phone: 917-376-2270
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Freiburg Mindfulness Inventory (FMI) Score at Baseline; Freiburg Mindfulness Inventory (FMI) Score at Post-Intervention Assessment; International Physical Activity Questionnaire (IPAQ) Score at Baseline; International Physical Activity Questionnaire Score at Post-Intervention Assessment; Health Promoting Lifestyle Profile II (HPLP-II) Score at Baseline; Health Promoting Lifestyle Profile II (HPLP-II) Score at Post-Intervention Assessment; Connor-Davidson Resilience Scale 10 (CD-RISC-10) Score at Baseline; Connor-Davidson Resilience Scale 10 (CD-RISC-10) Score at Post-Retention Assessment; Perc...
Can't join this trial?
Data last synced from ClinicalTrials.gov: 22 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.