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Patient-Centred Perioperative Mobile Application

Patient-Centered Perioperative Care Through Mobile Application: Patient Engagement Prospective Cohort Study in Elective Cesarean Delivery Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03746678
Enrollment
36
Registered
2018-11-20
Start date
2018-11-19
Completion date
2019-04-01
Last updated
2018-11-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cesarean Delivery

Keywords

Cesarean delivery, Perioperative medicine, Mobile health

Brief summary

With increasingly more complex surgical patients and the trend toward decreased hospital stay after operations, continuity of care and prompt management of symptoms and side effects perioperatively are ever more crucial. The investigators' goal is to improve perioperative care with a patient-centred mobile application, starting with a pilot in patients undergoing elective Cesarean delivery. The investigators have completed a research study where they created a prototype based on feedback from patients and anesthesiologists. In this study, the investigators would like to learn about how patients use our mobile application after delivery and how the mobile application can be integrated into daily practice.

Detailed description

The objective of this cohort study is to build the mobile application and evaluate its feasibility in providing patient education and reminders for self-monitoring for cesarean delivery patients. The investigators will measure the extent of patient engagement with our application through in-app usage data, as well as receive quantitative and qualitative feedback regarding feasibility. By understanding user behavior and needs through questionnaires and application usage data, the investigators could design more effective and tailored interventions for patients. Results of this study will help further development and implementation of an interdisciplinary mobile monitoring and communication platform for perioperative care. This study is funded by the Dalhousie University Department of Anesthesia, Pain Management & Perioperative Medicine.

Interventions

OTHERC-Care Mobile Application

C-care is a mobile application developed based on previous research at the IWK Health Centre. It contains topics relevant to Cesarean delivery and the recovery process, which the patient could access at anytime. Patient engagement with the application will be monitored anonymously for 30 days after delivery. On days one to five after delivery, patients will receive a short self-monitoring questionnaire (approximately 1 minute). At the end of two weeks (14 days), patients will complete an online survey regarding overall satisfaction, potential impact on care, usability and feasibility problems. At any point during the study, patients can email us to report any problems with the application.

Sponsors

IWK Health Centre
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Part 1 (screened by asking nurse) * Patient scheduled for elective Cesarean delivery * Age equal or greater than 18 * American Society of Anesthesiologists (ASA) Physical Status I-III (i.e. not in life-threatening situation) Part 2 (screened in person) * Possesses an iOS Smartphone with active data plan and access to WiFi, and self-reported use of it on a regular basis (at this stage in development, the mobile application prototype is only available on iOS) * Self-reported proficiency with Smartphone and mobile applications * Reported fluency in English

Exclusion criteria

Self-reported physical or psychiatric condition that may impair the ability to use the mobile application, answer questionnaires and surveys, and/or provide insights representative of the general population, such as blindness, under current influence of recreational drugs or alcohol.

Design outcomes

Primary

MeasureTime frameDescription
Median number of information topics viewed per participant30 daysQuantitative mobile application usage data
Median number of self-monitoring questionnaires completed per participant30 daysQuantitative mobile application usage data
Median number of total visits to the mobile application per participant30 daysQuantitative mobile application usage data
Satisfaction score (scale of 0 to 10, 10 being extremely satisfied, 0 being not satisfied)2 to 3 weeksQuantitative responses from survey
Percentage of participants who would recommend the C-Care App to other women undergoing Cesarean delivery2 to 3 weeksQuantitative responses from survey
Percentage of self-monitoring questionnaires completed (out of 5) per participant30 daysQuantitative mobile application usage data

Secondary

MeasureTime frameDescription
Median duration (number of days starting from delivery date until the last day of visit) patient interacted with application.30 daysQuantitative mobile application usage data
% participant who responded yes to the question that C-Care App provided them with knowledge about Cesarean delivery and anesthesia2 to 3 weeksQuantitative responses from survey
% participant who responded yes to the question that C-Care App provided them with knowledge about potential complications to monitor for2 to 3 weeksQuantitative responses from survey
% participant who responded yes to the question that C-Care App provided them with knowledge about the recovery process after Cesarean delivery2 to 3 weeksQuantitative responses from survey
Which topics were viewed the most (rank by topic name and by postoperative day)30 daysQuantitative mobile application usage data
If the patient did not use the mobile application, what were the reasons?2 to 3 weeksQualitative responses from survey
How could we make the mobile application more helpful for the patient?2 to 3 weeksQualitative responses from survey
What do patients think about the name of this App, C-Care? Do they have any other suggestions for our name/logo?2 to 3 weeksQualitative responses from survey
Any other comments and/or suggestions2 to 3 weeksQualitative responses from survey
Anything the patient wanted to change about this application, in terms of content, navigation, appearance, and overall experience?2 to 3 weeksQualitative responses from survey
Which self-monitoring questionnaires were filled the most (rank by postoperative day number)30 daysQuantitative mobile application usage data
Incidence of important potential anesthetic-related problems entered by the patient (pain, headache, weakness and numbness)30 daysQuantitative mobile application usage data
Time of the day patient visited site (scatter plot of Nova Scotia time vs. # visits) - one visit = at least one interaction within app, e.g. opening a topic, navigating within app30 daysQuantitative mobile application usage data
Time of the day patient filled out the questionnaire30 daysQuantitative mobile application usage data
Number of visits vs. postoperative day30 daysQuantitative mobile application usage data

Countries

Canada

Contacts

Primary ContactJanny X Ke, MD
AnesthesiaResearch@iwk.nshealth.ca(902) 470-7473
Backup ContactRonald B George, MD FRCPC
AnesthesiaResearch@iwk.nshealth.ca(902) 470-7473

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026