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Patient-reported Outcomes for Patients Undergoing Surgery at Shouldice Hospital.

Hernia

Background:

Previous publications have highlighted limited data on patient outcomes and experiences at Shouldice Hospital. Existing studies from Europe reported outcomes following Shouldice repair but lacked recent data. The current project seeks to optimize patient care and knowledge through systematic follow-up.

Study Objectives:

Establish a patient-reported outcome measure follow-up program. Evaluate postoperative complication rates. Determine important outcomes to patients. Establish and monitor patient satisfaction with decision-making and hernia repair.

Hypotheses/Research Questions:

Several research questions related to patient motivations, outcomes, knowledge, and satisfaction are posed for investigation.

Potential Risks and Benefits:

No anticipated risks to participants. Participants won't directly benefit but contribute to improving patient care and knowledge.

Study Design:

The study employs a prospective follow-up approach. Surveys are sent at specific intervals (30-40 days, 1-year, 3-years, and 5-years) via email.

Consent forms are included in the email, allowing participants to choose their level of involvement. Data is collected from survey responses, patient charts, and operative notes.

Study Population:

All patients aged 16-90 who underwent hernia surgery at Shouldice Hospital are eligible.

Exclusion criteria:

Lack of an email address. The required sample size is unknown, and this study serves as a pilot.

Data Collection:

Data is collected from surveys, patient charts, and operative notes. Consent is obtained through deferred consent (initial contact via email, with consent forms provided).

Safeguards are in place to protect personal health information.

Duration of Study:

Estimated to take 5-6 years. Recruitment/enrollment: 6-12 months. Follow-up: 5 years from the last enrolled participant. Data analysis and write-up: 5 months.

Overlap with Other Projects:

Concerns about overlap with other studies are addressed, and concurrent participation is allowed. Participants can withdraw at any time.

In summary, this research project aims to gather comprehensive data on hernia surgery outcomes, patient experiences, and satisfaction at Shouldice Hospital through a systematic follow-up approach, contributing to the improvement of patient care and knowledge in this field.

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    16 and up

Participation Criteria

Inclusion Criteria:

* All patients aged 16-90 who underwent hernia surgery at Shouldice Hospital are eligible.

Exclusion Criteria:

* Lack of an email address.

Study Location

Shouldice Hospital
Shouldice Hospital
Thornhill, Ontario
Canada

Contact Study Team

Backup Contact

Fernando Netto Spencer, PhD

[email protected]
905-889-1125 ext. 1297
Primary Contact

Marguerite Mainprize, MSc

[email protected]
905-889-1125 ext. 1297
Study Sponsored By
Shouldice Hospital
Participants Required
More Information
Study ID: NCT06039800