ClinicalTrials.Veeva

Menu

Preoperative Rehabilitation and Education Program (PREPS)

L

Lawson Health Research Institute

Status

Not yet enrolling

Conditions

Shoulder Arthritis
Patient Education
Shoulder Arthroplasty
Prehabilitation

Treatments

Other: Experimental: PREPS and therapy
Other: Experimental: PREPS only

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Shoulder problems affect many Canadians yearly. While surgery is one of the best treatments for shoulder problems, patients are unaware about shoulder replacement surgeries, the exercises needed after surgery and how to safely recover from the surgery without having another injury. Uncertainties about the surgery and recovery process can further cause post-surgery problems such as: pain, anxiety and re-injury. While some healthcare centers offer an in- class program to educate patients before surgery, some patients face issues with distance or transportation, and cannot regularly meet their doctor to address all their concerns. This project aims to create an online educational program that will teach patients through online videos and educational materials before they go into shoulder replacement surgery. By creating online modules, it can increase the accessibility for home use, and prepare patients on topics such as: their concerns about the surgery and proper exercises they can expect after surgery for a safe recovery. The aim is to study three groups of patients before surgery; 1. a group consisting of an online pre-rehabilitation program 6 weeks before surgery, 2. a group consisting of an online pre-rehabilitation program 6 weeks before surgery + therapist or 3. A group consisting of the current standard of care, which is a WebEx pre-operative education class lead by a physiotherapist and occupational therapist. Researchers will monitor all groups on their recovery before and after surgery. This will provide another alternative to informing patients before surgery and help them to prepare better for surgery. The online modules will contribute to improving the care in Southern Ontario and eventually be used for future care across Canada.

Full description

A total shoulder replacement is a common procedure to help those with shoulder osteoarthritis improve their quality of life. There is a lack of quality research on the effectiveness of prehabilitation and education on pain, function, and quality of life in patients undergoing this procedure. Researchers have developed a comprehensive, patient-centered program that combines exercise, preparedness for surgery, motivational interviewing, and pain management principles, in collaboration with patient partners on the wait list for a shoulder replacement, transdisciplinary healthcare team (i.e., surgeons, physiotherapists, occupational therapists, and rehabilitation researchers), and current scientific literature. This patient-centered program has the potential to improve postoperative pain, function, and patient-oriented outcomes, decrease postoperative opioid use and short and long-term healthcare costs. This pilot randomized controlled trial will evaluate feasibility and satisfaction of the program for individuals undergoing a shoulder replacement. Participants (n=90) undergoing a shoulder replacement will be randomized into 1) 6-week online pre-rehab and education program, 2) 6-week online pre-rehab and education program with a therapist or 3) standard of care group. The intervention groups will be delivered virtually with an online program of modules and a written handbook for participants. Participants in the standard of care group will receive usual care. Outcomes will be assessed at baseline and 1 day before surgery, then post-operatively at 6 weeks, 3 months, 6 months and 12 months.

Enrollment

90 estimated patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Over the age of 18 years old
  • Patients who have consented for a total shoulder arthroplasty or reverse shoulder arthroplasty surgery at HULC.
  • Date of surgery must be no shorter than 9 weeks, to ensure time for baseline measures
  • Speaks and reads in English unless can provide a translator
  • Able to provide informed consent.
  • Willing to participate in study procedures for at least 1 year post-surgery.

Exclusion criteria

  • Patients who have consented for a hemi-arthroplasty surgery
  • Patients who have been consented less than 8 weeks before surgery
  • Any contraindications to exercise

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

90 participants in 3 patient groups

Standard of Care Group
No Intervention group
Description:
A group consisting of the current standard of care at HULC, which is a WebEx pre-operative education class lead by a physiotherapist and occupational therapist.
Online only
Experimental group
Description:
a group consisting of an online pre-rehabilitation program 6 weeks before surgery
Treatment:
Other: Experimental: PREPS only
Online and PT
Experimental group
Description:
a group consisting of an online pre-rehabilitation program 6 weeks before surgery + therapist
Treatment:
Other: Experimental: PREPS and therapy

Trial contacts and locations

1

Loading...

Central trial contact

Joy MacDermid, PhD; Katrina Munro

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems