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A Study on the Use of Educational Programs Prior to Lumbar Spinal Surgery

A Prospective Randomized Control Trial Assessing the Effect of Two Different Educational Programs on Functional Outcome and Quality of Life Scores for Patients Having Posterior Decompressive Lumbar Spinal Surgery for Degenerative Conditions of the Lumbar Spine

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00719485
Enrollment
70
Registered
2008-07-21
Start date
2009-04-30
Completion date
2011-02-28
Last updated
2009-02-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Decompression, Surgical

Keywords

lumbar decompression

Brief summary

This study evaluated the hypothesis that the implementation of an educational program that informs spine patients about their condition, treatment options, prioritization on the wait list, and post-operative care would improve functional outcome and quality of life scores following surgery

Detailed description

Previous literature has shown that longer waits to lumbar spine surgery can have negative effects on the patients perceived function and quality of life both pre- and post-operatively. Patients report deterioration during this long wait, commonly over 6 months in Ontario. The proposed study intends to evaluate the impact of two different educational methods for patients undergoing lumbar spine surgery. This prospective randomized clinical trial will assign patients to two different educational groups: one of solely standard care, and the other of standard care with the addition of presentation of a 10 minute educational video informing spine patients about their condition, treatment options, prioritization on the wait list and post-operative care. Outcome measures will be assessed through four different questionnaires concerning specific conditions, pain, quality of life, etc., both pre-operatively and post-operatively. Providing patients with this accurate information may coincide with positive outcome measures. The more successful educational program, as found by this study, may then be provided to all spine patients. This educational program may bring about an increase in overall well-being of spine patients by having a positive impact on the quality of life both pre- and post-operatively.

Interventions

OTHEREducational program

Informing patients about their condition, treatment options, prioritization on the wait list, and post-operative care

Sponsors

Sunnybrook Health Sciences Centre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Degenerative condition of the lumbar spine requiring decompressive surgery

Exclusion criteria

* emergent spinal condition * acute bowel/bladder dysfunction * cervical spine condition * inability to participate in follow up and/or functional tests or questionnaires during study timeline (due to substance abuse, etc...) * revision surgery

Design outcomes

Primary

MeasureTime frame
Functional outcome scores2 years following surgery

Secondary

MeasureTime frame
Quality of life scores2 years following surgery

Contacts

Primary ContactAlbert Yee, MD
albert.yee@sunnybrook.ca416-480-6815

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026