The Single Assessment Numeric Evaluation (SANE) for Lumbar Discectomy

Sponsor
Windsor-Essex Compassionate Care Community (Other)
Overall Status
Recruiting
CT.gov ID
NCT05070078
Collaborator
(none)
400
1
13
30.8

Study Details

Study Description

Brief Summary

In the last several decades, many Patient Reported Outcomes Measures (PROMs) have been developed to provide assessment of patient health across multiple domains, as they relate to various spine conditions. However, many of the available PROM surveys have many questions and require substantial time to complete and/or assess one focal domain of health requiring multiple tools to achieve an overall assessment of well-being. Thus, concerns have arisen regarding patient survey fatigue and data integrity.

The Single Assessment Numeric Evaluation (SANE) is a single-question outcome measure that asks patients to rate their function, as it pertains to the area being treated, on a scale of 0 to 100. The SANE score has excellent acceptance in some orthopedic surgery research, where it has been shown responsiveness similar to more comprehensive legacy measures. The SANE thus eliminates survey fatigue and has been validated across a spectrum of orthopedic subspecialties. To our knowledge, however, the SANE has never been studied in a patient population undergoing any type of spinal surgery. Thus, we set out to compare the SANE score in patients undergoing lumbar discectomy to currently utilized PROM scores, including the Oswestry Disability Index (ODI), Zurich Claudication Scale (ZCS), and short form-36 (SF-36).

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Background/Rational: In the last several decades, many Patient Reported Outcomes Measures (PROMs) have been developed to provide assessment of patient health across multiple domains, as they relate to various spine conditions. When considered in concert, these instruments quantify and stratify an individual's health state before and after surgery and can be utilized to perform research as well as inform clinical practice. However, many of the available PROM surveys have many questions and require substantial time to complete and/or assess one focal domain of health requiring multiple tools to achieve an overall assessment of well-being. Thus, concerns have arisen regarding patient survey fatigue and data integrity. Ideally, a PROM would provide sufficient information to define health status longitudinally, while requiring the least amount of time and effort to complete. The current approach to PROMs in spine surgery research has been mostly to require an assessment of pain, disease specific disability and general health, requiring answers for up to of 40 unique questions, despite efforts to shorten the questionnaires in other neurosurgery and orthopedics disciplines.

    The Single Assessment Numeric Evaluation (SANE) score is one such example of a limited question survey that aims to assess multiple domains. The SANE is a single-question outcome measure that asks patients to rate their function, as it pertains to the area being treated, on a scale of 0 to 100. The SANE score has excellent acceptance in some orthopedic surgery research, where it has been shown responsiveness similar to more comprehensive legacy measures. The SANE thus eliminates survey fatigue and has been validated across a spectrum of orthopedic subspecialties. To our knowledge, however, the SANE has never been studied in a patient population undergoing any type of spinal surgery. Thus, we set out to compare the SANE score in patients undergoing lumbar discectomy to currently utilized PROM scores, including the Oswestry Disability Index (ODI), Zurich Claudication Scale (ZCS), and short form-36 (SF-36).

    Design: Survey research design, prospective outcomes measure validation study.

    Objectives: We hypothesized that the SANE score would correlate strongly and demonstrate similar magnitudes of longitudinal responsiveness with the more lengthy and burdensome legacy PROMs used in spine surgery research today.

    Primary Objective: To correlate and confirm that SANE score to the more lengthy and burdensome legacy PROMs used in spine surgery research today.

    Secondary Objective: There are multiple secondary aims of this study as shown below.

    1. Evaluate patients' satisfaction after surgery.

    2. Assess efficacy of treatment over time.

    3. Evaluate patients' sense of functional improvement after lumbar disc procedures.

    Information gained from this study will greatly enhance our ability to know whether SANE correlates with PROMS. Although the results of the trial will not directly benefit all the individuals participating, information gathered from this study can help future patients by reducing the burden of completing lengthy surveys and minimizing survey fatigue.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    400 participants
    Observational Model:
    Other
    Time Perspective:
    Prospective
    Official Title:
    The Single Assessment Numeric Evaluation (SANE): Is a Reliable Metric to Measure Clinically Significant Improvements After Lumbar Discectomy
    Actual Study Start Date :
    Nov 10, 2021
    Anticipated Primary Completion Date :
    Dec 10, 2022
    Anticipated Study Completion Date :
    Dec 10, 2022

    Outcome Measures

    Primary Outcome Measures

    1. Correlation of SANE score [November 2022]

      To correlate and confirm that SANE score to the more lengthy and burdensome legacy PROMs used in spine surgery research today. Spearman's correlation and linear regression will be performed for each time point, and for the change from preoperative to final follow up to validate the SANE as compared to the other PROMs.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patient over 18 years of age undergoing a lumbar discectomy.
    Exclusion Criteria:
    • Previous history of lumbar surgery.

    • Pediatric age group.

    • Patients with a postoperative follow-up time of less than 1 year.

    • Unstable patients in need of fixation.

    • Patients with cauda equina syndrome.

    • Non-compliant patients.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Windsor Regional Hospital - Ouellette Windsor Ontario Canada N9A 1E1

    Sponsors and Collaborators

    • Windsor-Essex Compassionate Care Community

    Investigators

    • Principal Investigator: Mohamed Soliman, Cairo University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Mohamed Soliman, Neurosurgeon, Principal Investigator, Windsor-Essex Compassionate Care Community
    ClinicalTrials.gov Identifier:
    NCT05070078
    Other Study ID Numbers:
    • 21-409
    First Posted:
    Oct 6, 2021
    Last Update Posted:
    Apr 27, 2022
    Last Verified:
    Apr 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Mohamed Soliman, Neurosurgeon, Principal Investigator, Windsor-Essex Compassionate Care Community

    Study Results

    No Results Posted as of Apr 27, 2022