About this trial
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
All patients aged 16-90 who underwent hernia surgery at Shouldice Hospital are eligible.
Disqualifiers
Lack of an email address.
Trial population
The study will include all patients aged 16-90 who underwent hernia surgery at Shouldice Hospital, with the only exclusion being those without an email address. This exclusion is due to the electronic nature of the project. Since this is the first study of its kind at Shouldice Hospital, the required sample size is unknown, and this project serves as a pilot for systematic follow-up on patient and surgical outcomes. For the specific analysis of infection rates, the study aims to gather data from 2,000 patients. To achieve this, the researchers plan to contact 4,500 patients, based on information from previous projects. Initial research contact yielded a 45% response rate, and no dropout rate has been measured yet, as data collection for this study will inform future sample size calculations.
Trial design
Other
Prospective
Treatments tested in this trial
No intervention
Other interventionNo intervention
Treatment groups
Trial outcomes
Primary outcomes
Recurrence after hernia repair
Recurrence after hernia repair
Secondary outcomes
Recurrence after hernia repair
Recurrence after hernia repair
Recurrence after hernia repair
Recurrence after hernia repair
Recurrence after hernia repair
Recurrence after hernia repair
Sponsors and contacts
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