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Virtual Reality Cognitive Intervention for Critically Ill Delirium Survivors (VR-Cog)
Recruiting
Who can join
Ages 50 and older · All sexes
Full eligibility criteria
Inclusion Criteria: * Adults aged 50 years or older * English speaking * Admitted to the intensive care unit (ICU) with acute respiratory failure/invasive mechanical ventilation * Screening positive for delirium (using Richmond Agitation Sedation Scale and Confusion Assessment Method for the ICU) Exclusion Criteria: * Acute neurologic injury such as stroke, traumatic brain injury, brain mass, intracranial hemorrhage, seizures, or central nervous system infection * Chronic cognitive or physical function deficit preventing participation in study interventions or assessments (determined by chart diagnoses and direct participant interview) * Chronic cognitive impairment (including mild cognitive impairment or dementia) identified by chart diagnosis, prescription of anti-dementia medications, or Informant Questionnaire on Cognitive Decline in the Elderly Score (IQCODE) \>3.3 obtained from family caregiver * Severe, uncorrected vision or hearing impairment preventing participation in intervention or outcomes assessments * Admitted with acute alcohol or drug intoxication or withdrawal * Severe, uncontrolled psychiatric disorder (bipolar disorder or schizophrenia) * History of severe vertigo, motion-induced sickness, headaches, light sensitivity, seizures, or prior intolerance of virtual reality (VR) * Receiving comfort care measures or not expected to survive the hospitalization * Prisoners or patients unable to provide consent * Not expected to be discharged home from the hospital, or living more than 50 miles from the nearest recruitment site, or homeless
About the study
The purpose of this study is to measure the feasibility, acceptability of virtual reality (VR) brain games and estimate their effect on memory, attention, and mood for ICU survivors. The VR program will be used at home through a headset and hand controls.
What is being tested
- VR-based cognitive training program (device)
- VR-based attention control (device)
Sponsor: Indiana University · Participants: 100 · Started: Mar 19, 2026
Contact the study team
- Sikandar Khan, DO, MS · Phone: (317) 274-9427
- Lori Rawlings, RN, BSN · Phone: 317-274-9052
Official record on ClinicalTrials.gov — NCT07496255
Locations in the U.S.
| Indiana | IU Health Methodist Hospital, Indianapolis |
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.