RECRUITING

The Impact of Prehabilitation

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

While numerous studies have assessed the promising impacts of prehabilitation, there is a lack of prehabilitation research within lower socioeconomic patient populations. Often for prehabilitation studies, patients are heavily involved in full scale exercise and nutrition programs weeks before the scheduled procedure. In underserved populations, programs such as these are often not feasible due to lack of transport, resources, and other barriers to healthcare. The investigators seek to evaluate the effectiveness of inexpensive interventions in lower socioeconomic populations. The investigators hypothesize that barriers to prehabilitation are environmental and that prehabilitation interventions tailored for lower socioeconomic (SES) populations will improve time to discharge, mobility, and in turn, readmission rates. The participants for this clinical trial will be seen four times: initially at the preoperative surgical clinic (6-8 weeks prior to surgery), 1-2 days preop at a pre-procedure clinic, postoperative in the inpatient setting (as soon as the participant is able to ambulate during their hospital stay), and in the postoperative surgical clinic at the postoperative visit. Patients will be within the general surgery, colorectal, and surgical oncology departments at Boston Medical Center (BMC). The anticipated sample size is 60 participants (30 in the intervention/prehabilitation arm and 30 in the control/usual care arm). Participants in the intervention arm will participate in a mobility and step tracking intervention aimed at improving postoperative outcomes. The control group will follow routine standard of care at BMC for preoperative and postoperative care.

Official Title

The Impact of Prehabilitation Measures on Postoperative Outcomes

Quick Facts

Study Start:2024-05-02
Study Completion:2025-03
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06181253

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:21 Years to 65 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients within general surgery, colorectal, and surgical oncology departments at Boston Medical Center.
  2. * English or Spanish speaking
  3. * Able to ambulate without cane, walker, wheelchair
  4. * Surgery scheduled within 4-8 weeks
  5. * Must have cell phone with internet access and text message capabilities
  6. * JH-HLM score of 6
  1. * Limited/non readers (less than 5th grade reading level), assessed via comprehension of consent materials

Contacts and Locations

Study Contact

Nicole Spence, MD
CONTACT
617-638-6950
Nicole.Spence@bmc.org
Vaibhav Gupta, BA
CONTACT
617-638-6950
vgupta21@bu.edu

Principal Investigator

Nicole Spence, MD
PRINCIPAL_INVESTIGATOR
Boston Medical Center, Anesthesiology Department

Study Locations (Sites)

Boston Medical Center
Boston, Massachusetts, 02118
United States

Collaborators and Investigators

Sponsor: Boston Medical Center

  • Nicole Spence, MD, PRINCIPAL_INVESTIGATOR, Boston Medical Center, Anesthesiology Department

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-05-02
Study Completion Date2025-03

Study Record Updates

Study Start Date2024-05-02
Study Completion Date2025-03

Terms related to this study

Keywords Provided by Researchers

  • Prehabilitation
  • Patient video education
  • Instructional walking video
  • 6 minute Walking test
  • Patient texting

Additional Relevant MeSH Terms

  • Post Operative Complications