COgnitive and Physical Exercise (COPE) Prehabilitation Pilot Feasibility Study
Cognitive Impairment, Physical Impairment, Postoperative Complications
About this trial
This is an interventional prevention trial for Cognitive Impairment
Eligibility Criteria
Inclusion Criteria:
- Adults undergoing major surgery with the likelihood of prolonged hospitalization or critical illness among the following surgical services: general surgery, surgical oncology, otolaryngology, hepatobiliary, thoracic, and vascular surgery
Exclusion Criteria:
- Blind, deaf, or unable to speak English, as these conditions would preclude our ability to perform the proposed cognitive and physical program
- Pregnancy
- Prisoners
- Severe frailty or physical impairment that prohibits participation in prehabilitation program
- Patients with documented dementia or cognitive impairment that precludes ability to self-consent for surgery and study participation
- Less than 2 weeks from scheduled surgery
- Patients without home internet access
Sites / Locations
- Vanderbilt University Medical Center
Arms of the Study
Arm 1
Arm 2
Other
Experimental
Control
Cognitive and physical prehabilitation
The active attention control group will receive a binder with information about personal health including sleep hygiene, nutritional changes, and stress reduction. In addition, they will participate in a control version of the cognitive training program. They will receive weekly phone calls by cognitive and physical therapy teams to address issues with any aspects of the program.
The intervention group will receive the prehabilitation program consisting of a guided progressive program of home-based aerobic and resistance training exercise, which will be adapted based on kinesiologist recommendation for each individual and the individual's perceived exertion. In addition, they will have access to the full cognitive training program. They will receive weekly phone calls by cognitive and physical therapy teams to address issues with any aspects of the program.