[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100556253":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":22,"centralContacts":26,"locations":37,"responsibleParty":54,"collaborators":30,"id":57,"slug":58,"hasResults":59,"nctId":60,"briefTitle":61,"officialTitle":62,"acronym":63,"eligibilityCriteria":64,"healthyVolunteers":59,"sex":65,"minAge":66,"maxAge":30,"enrollmentInfo":67,"targetDuration":30,"studyType":70,"phases":71,"briefSummary":73,"conditions":74,"keywords":77,"overallStatus":84,"whyStopped":30,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":89,"completionDateStruct":91,"leadSponsor":93,"locationsCount":94},{"fullName":5,"class":6},"Ciusss de L'Est de l'Île de Montréal","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Smart Pill Bottle Data Collection Group","EXPERIMENTAL","Group of patients in which data on postoperative opioid medication consumption will be collected through the use of smart pill bottles.",[13],"Device: Smart Pill Bottle",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"DEVICE","Smart Pill Bottle","Patients in the intervention group will have their opioid medication consumption monitored through a smart pill bottle that records medication usage and streamlines the data into an online platform accessible by the medical staff. This group will also fill out surveys delivered through the smart pill bottle's online platform.",[9],[21],"Connected Pill Bottle",[23],{"name":24,"affiliation":5,"role":25},"Pascal Laferriere-Langlois, MD, MSc","PRINCIPAL_INVESTIGATOR",[27,32],{"name":24,"role":28,"phone":29,"phoneExt":30,"email":31},"CONTACT","+1-819-432-5847",null,"pascal.laferriere-langlois@umontreal.ca",{"name":33,"role":28,"phone":34,"phoneExt":35,"email":36},"Nadia Godin, NR","514-252-3400","3193","ngodin.hmr@ssss.gouv.qc.ca",[38],{"facility":39,"status":30,"city":40,"state":41,"zip":42,"country":43,"countryCode":44,"cosmosGeoPoint":45,"geoPoint":50,"contacts":51},"Maisonneuve-Rosemont Hospital - CIUSSS de l'Est de l'Île de Montréal","Montreal East","Quebec","H1T2M4","Canada","CA",{"type":46,"coordinates":47},"Point",[48,49],-73.5075,45.63202,{"lat":49,"lon":48},[52,53],{"name":24,"role":28,"phone":29,"phoneExt":30,"email":31},{"name":24,"role":25,"phone":30,"phoneExt":30,"email":30},{"type":25,"investigatorFullName":55,"investigatorTitle":56,"investigatorAffiliation":5,"oldNameTitle":30,"oldOrganization":30},"Pascal Laferrière-Langlois","Clinical assistant professor","100556253","optimizing-research-data-acquisition-with-smart-pill-bottles-100556253",false,"NCT06522698","Optimizing Research Data Acquisition With Smart Pill Bottles","Optimizing Research Data Acquisition With Smart Pill Bottles: A Feasibility and Implementation Study","SPB","Inclusion Criteria:\n\n* All consenting adult patients (age \\>17 years) undergoing major abdominal surgery via laparotomy (any open surgery involving the abdominal compartment or its wall, excluding appendectomies, inguinal hernia repairs, abdominal wall hernia repairs, and incisional hernia repairs)\n\nExclusion Criteria:\n\n* Patients enrolled in the historical cohort (POCAS study)\n* Patients currently participating in another study\n* Patients planned to undergo additional surgery within 90 days after the surgery\n* Patients who do not understand French or English.\n* Patients planned to be redirected to a secondary care or rehabilitation establishment following discharge\n* Patients with diagnosed cognitive impairment","ALL","18 Years",{"count":68,"type":69},155,"ESTIMATED","INTERVENTIONAL",[72],"NA","The goal of this clinical trial is to learn if smart pill bottles can be used as a tool to optimize data collection in clinical trials by increasing the quality of data collected and limiting the associated cost. The main questions it aims to answer are:\n\nIs the use of smart pill bottles a feasible method of data collection in clinical trials in terms of patient adherence.\n\nIs the data collected by the smart pill bottles of higher quality than that collected through human resources? What is the impact of the use of smart pill bottles on the costs involved in clinical trials ?\n\nResearchers will collect data on postoperative opioid medication consumption with the smart pill bottle and assess the adherence of patients to the device along with the quality of data collected and the costs involved in the process.\n\nParticipants will:\n\nUse the smart pill bottle to consume opioid medication following surgery for 3 months At the end of the 3 month period, the group will have filled out surveys detailing their opioid consumption, surgical pain and other relevant information.",[75,76],"Post Operative Pain","Opioid Use",[78,79,80,81,82,83],"Major abdominal surgery","Connected Technology","Chronic Pain","Postoperative pain","Opioid consumption","Smart Pill Bottles","NOT_YET_RECRUITING","2024-07-25",{"date":87,"type":88},"2024-07-26","ACTUAL",{"date":90,"type":69},"2024-09-01",{"date":92,"type":69},"2025-07-01",{"name":5,"class":6},1]