Timing of Rehabilitation Following Cervical Spinal Surgery in Degenerative Myelopathy

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Alberta

About this trial

The goal of this clinical trial is to learn whether starting rehabilitation earlier after surgery can improve recovery and is feasible and acceptable for adults with degenerative cervical myelopathy (DCM) undergoing cervical spine surgery. The main question it aims to answer is:

Does starting rehabilitation earlier improve walking, balance, physical activity, quality of life, and nervous system function after surgery?

Researchers will compare participants who begin rehabilitation two weeks after surgery with participants who begin rehabilitation six weeks after surgery to see if earlier rehabilitation leads to better recovery outcomes and participation.

Participants will:

Be randomly assigned to begin rehabilitation either two weeks or six weeks after surgery.

Attend physical therapy sessions twice per week for eight weeks focused on strength, balance, and walking.

Complete assessments of walking ability, balance, physical activity, quality of life, and nervous system function over several months after surgery.

Provide feedback about their experience with the rehabilitation program, including satisfaction and any side effects or challenges related to participation.

Eligibility criteria

Qualifiers

adult (>18 years of age) with diagnosis of degenerative cervical myelopathy, within 2 weeks of spinal decompression surgery

plan to be discharged home from acute care (i.e., not admitted to another facility for post-operative rehabilitation)

able to stand with a maximum of one-person assist (+/- use of gait aid)

persistent functional impairment in lower extremity strength, balance, coordination, and/or gait

Disqualifiers

discharge from acute care facility > 2 weeks post-operative

intra-operative or early post-operative complication delaying discharge or precluding participation in early rehabilitation

Trial design

Treatments tested in this trial

  • Physical Therapy

Treatment groups

20 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

University of Alberta

Lead sponsor

Alberta Spine Foundation

Collaborator