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CompletedNCT05623813Updated Nov 21, 2022

Individual- and Group-based Postoperative Education for Patients Sternotomy

An observational study in Post-sternotomy, sponsored by University of Western Sydney. Completed. Open to participants aged 19 Years and older. Per ClinicalTrials.gov, last updated 2022-11-21.

Sponsored by University of Western Sydney · Observational

Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
88
Ages
19 Years and older
Sex
All
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Study 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.

Read the 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.

02

Conditions studied

  • Post-sternotomy

Keywords

  • patient education
  • individual and group delivery
  • engagement in daily activities
03

In context

Lead sponsor

University of Western Sydney is the lead sponsor of 9 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
19 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All patients aged 18 or above who had received cardiac surgery via sternotomy at Liverpool Hospital cardiothoracic ward.

Inclusion criteria

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

Exclusion criteria

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
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Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
88 participants (actual)
Patient registry
No

Groups and cohorts

  • Individual-based education

    Participants in the individual-based education would receive tailored education on sternal precautions to facilitate engagement in daily activities.

    Other: Postoperative education

  • Group-based education

    Participants in the group-based education would receive the same education on sternal precautions to facilitate engagement in daily activities.The group-based education included between two and five participants. They were invited to ask questions about their recovery and voice any concerns they had about being discharged home specific to their needs, covering a tailored portion of the education. Participants in group-based education had a chance to share their experiences and concerns with the group members.

    Other: Postoperative education

Interventions

  • OtherPostoperative education

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

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What researchers measure

Primary outcomes

  1. Survey

    On participants' understanding, confidence, and satisfaction of the education

    Time frame: Two to three days pre-discharge

  2. Survey

    On participants' understanding, confidence, and satisfaction of the education

    Time frame: Four to six weeks post-discharge

Secondary outcomes

  1. Time spent delivering education per participant

    The time spent for each session was measured in minutes using a timer from the start to the end of the education delivery

    Time frame: Post-discharge, up to six weeks

  2. Length of postoperative hospital stay

    Number of days between the date of surgery and the date of discharge

    Time frame: Post-discharge, up to six weeks

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: No — Individual participant data are not shared as per ethics protocol.

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 21, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05623813
Lead sponsor
University of Western Sydney
Collaborators
Liverpool Hospital
Responsible party
Karen Liu (Prof, University of Western Sydney) — Principal investigator
First posted
Nov 21, 2022
Start date
Aug 2016
Primary completion
Mar 2017
Completion
Aug 26, 2022
Last update
Nov 21, 2022

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2022. You cannot join it, but the record below documents what was studied.

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