- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05571566
The Impact of a Patient Education Tool for Appendicitis
The Impact of a Patient Education Tool on Parental Productivity and Anxiety: A Non-Randomized Control Trail
Hypothesis/Study question (brief introduction of the question studied; about 5 lines)
Appendicitis is the most common acute surgical admission to the pediatric surgery service at the MCH. The need for surgery can provoke anxieties for patients. Patient education materials are meant to improve knowledge, set expectations, and improve the overall hospital experience for patients and their families, and are already being widely implemented for elective surgeries in the context of ERAS pathways. This study aims to develop an effective patient and family education tool, with the goal of improving patient education and satisfaction with care in the emergency surgery setting.
Study objectives
- Utilize evidence-based methods to evaluate the success of implementation of a patient and family-centered education tool for appendicitis.
- Develop and validate a pre- and post- education patient satisfaction and experience survey in the realm of pediatric surgery.
- Inform the development of the education tool and survey through multidisciplinary and patient/family input.
- Implement a patient/family-centered education tool in an emergency surgical setting.
Study Overview
Detailed Description
Methodology / Study design
- Pilot phase Convenience sample of 10 patients diagnosed with acute appendicitis and their families will be selected to provide input on the patient and family experience survey tool. A convenience sample of 5 surgeons and 5 surgical nurses will also be solicited to provide feedback. The survey tool will be adapted based on the responses.
- Pre-implementation phase All patients and their families with acute appendicitis who present to clinic for their routine follow-up appointment or are called for their phone-call follow up will be eligible to take a survey. All responses are voluntary and anonymous. The survey swill be available on an online platform so invited participants may conveniently participate in the study.
- Post-implementation phase After the education pamphlet has been finalized and its distribution to families has begun, all patients and their families with simple or perforated appendicitis who had their initial presentation after the education pamphlet was available will be eligible to take a survey. All responses are voluntary and anonymous. The surveys will be available on an online platform so invited participants may conveniently and anonymously participate in the study.
Qualitative and descriptive statistics will be used to detect a difference in patient experience and satisfaction between the those who received the education tool and those who did not.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Quebec
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Montréal, Quebec, Canada, H4A 3J1
- Research Institute of the McGill University Health Center/ Montreal Children's Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Primary caregivers of all pediatric patients (0-17 years old) with acute appendicitis, including both perforated and non-perforated appendicitis cases, who have undergone an urgent appendectomy.
Exclusion Criteria:
- Patient or family does not understand English or French (education material available in only these two languages).
- Patient presenting for an elective interval appendectomy.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Non-Randomized
- Interventional Model: Sequential Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Pre-implementation phase
All patients with acute appendicitis who undergo appendectomies will be eligible to participate, and families will be consented prior to surgery.
The explanation of the procedure will be done verbally by the surgeon as it is the standard care at the hospital.
A parental anxiety assessment will be done before surgery with the Amsterdam Preoperative Anxiety and Information Scale (APAIS).
In addition, an email from one of the primary caregivers will be collected, and the caregiver will receive an email with a link to the post-operative questionnaire 10 days post-discharge.
At 14 days post-discharge, they will receive a reminder email again with the link to the questionnaire.
All responses to the questionnaire are voluntary and anonymous.
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|
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Active Comparator: Post-implementation phase
The education tool will be distributed to families whose child is undergoing an appendectomy.
The explanation of the procedure will also be done verbally by the surgeon as it is the standard care at the hospital.
The parental anxiety assessment will be done in the same way as above, before surgery with the Amsterdam Preoperative Anxiety and Information Scale (APAIS).
In addition, the email of one of the primary caregivers will be collected, and the caregiver will receive an email with a link to the post-operative questionnaire 10 days post-discharge.
At 14 days post-discharge, they will receive a reminder email with the link to the questionnaire.
All responses to the questionnaire are voluntary and anonymous.
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An educational book with information about appendicitis for patients, parents and caregivers
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Parental Anxiety
Time Frame: 1 hour - during surgery
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Scores from the anxiety scale from both phases - adapted from Parental Anxiety Scale based on Amsterdam Preoperative Anxiety and Information Scale (APAIS) - 9 questions. The Parental Anxiety score is a Likert scale with 6 questions (each 1-5). The cutoff for anxiety is 13 points, anything over it is High anxiety. |
1 hour - during surgery
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Parental Productivity
Time Frame: 10 & 14 days postoperatively
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Results from the online survey on parental productivity - adapted from Productivity and Disease Questionnaire (PRODISQ), the Health and Labor Questionnaire (HLQ) & additional literature. - 27 questions. The Parental Productivity survey will be a descriptive analysis and does not contain scoring. |
10 & 14 days postoperatively
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Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2019-5195
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Appendicitis
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