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Is a resistance exercise program following cardiac surgery safe and acceptable?

The safety and patient perceived acceptability of a resistance exercise program commenced during the early recovery period following cardiac surgery

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12625000313437
Enrollment
20
Registered
2025-04-16
Start date
2025-05-05
Completion date
2026-05-29
Last updated
2025-09-08

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

Conditions

None listed

Brief summary

This study will explore the safety of performing arm and leg exercises during the early recovery period following cardiac surgery. The exercises will be performed during weeks 2, 6 and 10 after surgery. The exercises will use no or minimal, inexpensive equipment and be performed to a light to moderate intensity. Safety will be established by measuring sternal (breastbone) edge micromotion during each upper limb exercise, and by monitoring pain and cardiovascular responses (for example, heart rate, pulse rhythm, blood oxygen levels and blood pressure). Participants will also be invited to participate in a 30-minute interview to explore their experience of engaging in the exercises and their perceived acceptability of people potentially performing the exercise at home without supervision in the future.

Interventions

Participants will engage in light to moderate upper and lower limb resistance exercises using no or minimal equipment such as body weight resistance elasticated exercise bands under supervision during three supervised sessions: one during week 2, one during week 6 and one during week 10 post-cardiac surgery. Each session will be 45 minutes in duration. The participants will not be asked to undertake these exercises at any other time during the study period. The exercises will be undertaken one-o

Participants will engage in light to moderate upper and lower limb resistance exercises using no or minimal equipment such as body weight resistance elasticated exercise bands under supervision during three supervised sessions: one during week 2, one during week 6 and one during week 10 post-cardiac surgery. Each session will be 45 minutes in duration. The participants will not be asked to undertake these exercises at any other time during the study period. The exercises will be undertaken one-on-one under the supervision of a physiotherapist. The exercises include bicep curls, shoulder flexion to 90 degrees, shoulder external rotation (with arms by the side), upright row, sit to stands, knee extensions, hamstring curls, calf raises, hip abduction and hip extension. At the week 10 session an additional exercise, wall pushups, will be added to the exercise protocol. Participants will perform 8-12 repetitions of each exercise at no greater than moderate intensity (5-6 out of 10 rating of perceived exertion or 4 repetitions in reserve). The primary objective of the study is to determine safety by measuring the amount of sternal edge movement occurring during the upper limb exercises at the three post-operative timepoints (weeks 2, 6 and 10). To assess sternal edge movement, during the upper limb exercises, the supervising physiotherapist will take ultrasound imaging recordings for analysis at a later stage to determine the amount of sternal edge movement taking place during each upper limb exercise. The supervising physiotherapist and the rest of the research team have all been trained in undertaking ultrasound sternal imaging. Secondary outcome measures to determine safety are pain and cardiovascular responses.

Sponsors

University of Otago
Lead SponsorUniversity

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

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

Inclusion criteria

Adults (18 years of age or over) awaiting either elective or emergency cardiac surgery (coronary artery bypass or heart valve surgery) at Dunedin Public Hospital who have no contraindications to participation in the opinion of the operating surgeon. Participants also need to live within a travelable distance (approximately 40 minutes) to the University of Otago, Dunedin to be able to take part in the in-person testing sessions.

Exclusion criteria

Significant post-operative medical complications (e.g., wound complications such as infection, severe pain or instability; and cardiovascular complications such as persistent cardiac arrhythmias or stroke). To ensure safety during the exercise testing, people will also be excluded from participation if they are unable to understand English or demonstrate impaired cognition and/or confusion. People with pre-existing muscle or joint problems that limit shoulder elevation up to 90° will be excluded from participating. People will also be excluded if they live too far away to travel to the testing facility (the research team have used up to 40-minute drive to invite people but people who live closer than this may still decide it is too far), or if they require taxi travel but live more than 20 km from the University of Otago (due to funding constraints). Participants may be withdrawn from the study by the operating surgeon at any time due to safety concerns.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026