ClinicalTrials.Veeva

Menu

Multi-Component Prehabilitation for Major Elective Surgery

Beth Israel Lahey Health logo

Beth Israel Lahey Health

Status

Completed

Conditions

Functional Recovery
Frailty
Prehabilitation

Treatments

Behavioral: Meditation
Behavioral: Cognitive Behavioral Intervention
Behavioral: Exercise
Behavioral: Nutrition

Study type

Interventional

Funder types

Other

Identifiers

NCT05752474
2022P000090

Details and patient eligibility

About

The purpose of this pilot study is to assess the feasibility of delivering a multicomponent prehabilitation and measuring patient-centered outcomes in older adults undergoing major surgery.

Full description

We will assess the feasibility of delivering a multicomponent prehabilitation, which consists of exercise (supervised by physical therapist), nutritional intervention (nutritional supplement and group education), meditation (group class), and cognitive behavioral intervention over 3-4 weeks before major elective abdominal, gynecological oncologic, urologic surgery, and cardiovascular procedures. We will also measure patient-centered outcomes (Patient-Reported Outcomes Measurement Information System) at 30 and 90 days after surgery. The target enrollment is 30 patients.

Enrollment

30 patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient is scheduled to have a gastrointestinal, gynecological oncologic, urologic, and cardiovascular procedure
  • Age 70 years+
  • Age 65 years+ AND high risk per surgeon's clinical judgment
  • Patient provides an informed e-consent or remote consent

Exclusion criteria

  • Surgery is scheduled less than 21 days
  • Patient is considered an inappropriate candidate per the surgeon's assessment
  • Non-English speaking
  • Major cognitive impairment
  • Patients with chronic kidney disease stage 3 or higher will be excluded from receiving protein supplement of the prehabilitation program

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

Prehabilitation
Experimental group
Description:
This group will receive a multicomponent prehabilitation intervention (exercise, nutritional intervention, meditation, and cognitive behavioral intervention) for 3-4 weeks prior to surgery.
Treatment:
Behavioral: Nutrition
Behavioral: Exercise
Behavioral: Cognitive Behavioral Intervention
Behavioral: Meditation

Trial documents
1

Trial contacts and locations

1

Loading...

Central trial contact

Dae Hyun Kim, MD, ScD; Natalie M Newmeyer, MS, RD, LDN

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems