Skip to content

Individual- and Group-based Postoperative Education for Patients Sternotomy

Individual- and Group-based Postoperative Education on Promoting Engagement in Daily Activities for Patients After Sternotomy: A Non-randomised Controlled Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05623813
Enrollment
88
Registered
2022-11-21
Start date
2016-08-31
Completion date
2022-08-26
Last updated
2022-11-21

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

Conditions

Post-sternotomy

Keywords

patient education, individual and group delivery, engagement in daily activities

Brief summary

Cardiac surgery via sternotomy is performed on more than one million people annually. Patient education may promote engagement in daily activities postoperatively. It is unknown if there is any difference in patients' feedback and outcomes when the education is delivered individually or in a group format. The aim of this study is to collect participants' feedback and therapists' time spent on individual- and group-based Education in Daily Activities Engagement - Post-Sternotomy.

Detailed description

This single-site non-randomised controlled study was conducted at Liverpool Hospital, NSW, Australia. All patients aged 18 or above who had received cardiac surgery via sternotomy at Liverpool Hospital cardiothoracic ward were consecutively allocated to the individual- or group-based postoperative education. Outcomes included a survey to obtain participants' feedback, the time spent by therapists delivering the education per participant, and participants' length of postoperative hospital stay.

Interventions

provide patients with the understanding and confidence to safely engage in their daily activities whilst following post-sternotomy precautionary guidelines throughout their recovery

Sponsors

Liverpool Hospital
CollaboratorUNKNOWN
University of Western Sydney
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* over the age of 18 * had received cardiac surgery via sternotomy * were medically ready for discharge

Exclusion criteria

* under the age of 18 * unable to provide consent * did not speak English * could not obtain a translator prior to discharge * were infectious and required to isolate

Design outcomes

Primary

MeasureTime frameDescription
SurveyTwo to three days pre-dischargeOn participants' understanding, confidence, and satisfaction of the education

Secondary

MeasureTime frameDescription
Time spent delivering education per participantPost-discharge, up to six weeksThe time spent for each session was measured in minutes using a timer from the start to the end of the education delivery
Length of postoperative hospital stayPost-discharge, up to six weeksNumber of days between the date of surgery and the date of discharge

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026