The Impact of Prehabilitation Bundle on Perioperative Outcome for Frail Elderly Patients Undergoing Major Abdominal Surgery
Complication, Postoperative, Perioperative/Postoperative Complications
About this trial
This is an interventional treatment trial for Complication, Postoperative focused on measuring Physiotherapy, Inspiratory Muscle Training, Perioperative Medicine, Postoperative outcomes, Preoperative nutrition, Elderly, frail
Eligibility Criteria
Inclusion Criteria:
- Patients attending the Preoperative Evaluation Clinic, SGH at least 11 days prior to his/her elective major abdominal surgery. Major abdominal surgery is defined as an intraperitoneal surgery with expected length of stay beyond 2 days. For patients who attended the clinic more than 11 days prior to surgery date, they will be informed to start their prehabilitation bundle 10 days prior to surgery.
- Aged 65 and above
- Diagnosed as frail based on Fried criteria score 3and above
- Able to understand and follow the prescribed cognitive and physical exercise
Exclusion Criteria:
- Patients with Parkinson disease, previous stroke, neuromuscular disorders and those taking carbidopa/levodopa, donepezil hydrochloride or antidepressants as previous studies have found that these medications may cause symptoms that are similar with domains of frailty.
- Patients who are not able to communicate
Sites / Locations
- Singapore General HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Active Comparator
No Intervention
Intervention
Control
In the interventional arm, patients will be given: A 'Threshold' Inspiratory Muscle Trainer A nutritional assessment: if needed, dietary supplements prescribed (i.e Ensure, Glucerna). Cognitive exercise in the form of the 'Memory' card game will be taught to the patients and the caregiver (if available), to be done twice a day. Patients will be provided with a protocol activities log and a study assistant will be conducting a telephone conversation on day 1, 4 and 7 to encourage compliance to the protocol and answer any queries with regards to the research study.
In the control arm, patients will be given the standard education materials regarding surgery and carry out daily activities as usual until the admission of the surgery.