Photographic Email Correspondence for Pediatric Urology Post-Operative Patients

Status: Completed
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

A pilot research study is planned to occur within the pediatric urology service the spring of 2015. All pediatric urology patients in the immediate post-operative period of 0-14 days will be eligible for this study. This study will compare the current standard of care for managing post-operative complications (a telephone conversation with the NP) versus an experimental intervention (telephone call and an electronic photograph of the surgical site). Before the surgical patient is discharged from the hospital, consent will be obtained for participation. Once a family initiates contact with the NP with a post-operative concern they will be randomized to either the control or the experimental group. Those in the control group will receive the current standard of care, which is telephone advice only. Those in the experimental group will speak to the NP on the telephone and will be requested to send an electronic photograph of their child's surgical site to the NP for assessment and advice. Photographs will be assessed using a standardized tool by both NPs and this information will be entered into a database. The investigators will be measuring the number of emergency department (ED) and/or unplanned clinic visits in both groups. An unplanned clinic visit is defined as a visit that is required due to an unexpected complication or concern before the original scheduled post-operative follow-up as determined by the surgeon. The investigators will be tracking the number of follow-up phone calls for both groups, as well as requiring participants to complete a family/patient experience survey after speaking to the NP.

Eligibility
Participation Requirements
Sex: All
Maximum Age: 18
Healthy Volunteers: No
View:

• Children aged 0-17 years who have undergone urological surgery.

• Children within the immediate post-operative period (0-14 days).

• Children with concerns directly related to operative site including, but not limited to catheters, stents, rashes and urine output.

Locations
Other Locations
Canada
McMaster Children's Hospital
Hamilton
Time Frame
Start Date: June 2015
Completion Date: February 2016
Participants
Target number of participants: 40
Treatments
Active Comparator: TTC
Current standard of care- a telephone call with the NP in the event of a post-operative concern where advice/interventions/reassurance is provided based on information provided by family
Experimental: PEC
Experimental arm, the standard telephone call with the NP and the addition of a digital photograph of the surgical site for assessment prior to the administration of advice
Sponsors
Collaborators: Hamilton Health Sciences Corporation
Leads: McMaster Children's Hospital

This content was sourced from clinicaltrials.gov

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