Prehabilitation in Elective Colorectal Resection: A Pilot Study (Prehab)

McMaster University

Status: Unknown

Conditions: Colorectal Cancer

Treatments: Other: Routine Care; Other: Physiatry Assessment

Study type: Interventional

Funder types: Other

Identifiers

NCT02531620

2015A1

Details and patient eligibility

About

This is a pilot study designed to evaluate a programme of rehabilitation for patients undergoing elective colorectal resection surgery.

Full description

Operations on the colon and rectum are major abdominal operations and many individuals can become severely deconditioned or weakened afterwards. For some individuals this can even mean that they can no longer completely return to their usual way of life following one of these major operations. As part of this study the investigators are attempting to identify ways to maximize patients' recovery and to maximize their overall quality of life following these major operations. It is possible that preconditioning may make a difference to patient's overall quality of life, decreased or need for hospital length of stay and decreased postoperative medical complications occasionally seen during these operations, in essence provide an overall enhancement to their surgical recovery. Physiatrists are physicians who are medical experts in maximizing a patient's overall ability to function well and live independently. Investigators are proposing patient participation in an initial pilot study in order to test the question as to whether or not participation with a physiatrist and any interventions recommended by said physician would help improve a patient's postoperative recovery.

Enrollment: 70 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• adult patient
• scheduled to undergo a colorectal resection as part of treatment for colorectal cancer.
• English speaking or have available a family member or substitute decision maker who can accompany you to all of your study visits.

Exclusion criteria

• geographic inaccessibility
• unwilling to provide consent

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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70 participants in 2 patient groups

Physiatry

Experimental group

Description:

Pre-operative Physiatry assessment and intervention

Treatment:

Other: Physiatry Assessment

Routine Care

Other group

Description:

Patients will receive routine pre-operative care, this study arm does not have an intervention.

Treatment:

Other: Routine Care