Skip to content

Water-based exercise in people with stable coronary heart disease (Study A)

A randomised, controlled trial of water-based exercise training in people with stable coronary heart disease (Study A)

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12616000113459
Enrollment
15
Registered
2016-02-02
Start date
2022-03-01
Completion date
Unknown
Last updated
2021-06-21

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

Conditions

None listed

Brief summary

Aims: The aim of this project is to assess the acute effects of water-based exercise in people with stable heart disease. This study is conducted in conjunction with a water-based training study to investigate the effects of water-based exercise training in people with stable coronary heart disease. Justification: Exercise is an important component of rehabilitation and preventing recurrent heart problems in people with heart disease. However, exercise participation is sub-optimal in this population and increasing the range of exercise options for people with heart disease may increase exercise participation. For example, water-based exercise may be more appealing to people with heart disease who have other health issues, such as arthritis or obesity, which may make land-based exercise difficult or painful. Furthermore, preliminary research suggests that water-based exercise may have additional vascular and brain benefits due to the effects of water immersion on blood flow. However, this has not previously been investigated in people with heart disease. Participants: Patients who have had a heart attack or bypass surgery at least six months prior to enrolment, or documented blockages in the arteries of their heart based on the results of an angiogram (a scan of the heart) will be recruited to the study. Participants must be medically stable prior to participation and not be undertaking a formal exercise program. Design and methods: This crossover study will compare the acute responses to low and moderate intensity exercise in the water with matched intensities on land. This will involve one endurance capacity assessment and one exercise session in 15 participants. The order of conditions will be randomised. Study A will acutely assess blood flow to the arm and brain, along with assessing systemic haemodynamics.

Interventions

This is a crossover study assessing acute physiological responses, including brain and arm blood flow and systemic haemodynamics, to low (40% VO2peak) and moderate (60% VO2peak) intensity water-based exercise and matched intensity land-based exercise. This will involve one endurance capacity assessment to determine VO2peak and one exercise session per participant, where they will take part in both land and water-based exercise in a randomised order, in the same session, with a 20-30minute break

This is a crossover study assessing acute physiological responses, including brain and arm blood flow and systemic haemodynamics, to low (40% VO2peak) and moderate (60% VO2peak) intensity water-based exercise and matched intensity land-based exercise. This will involve one endurance capacity assessment to determine VO2peak and one exercise session per participant, where they will take part in both land and water-based exercise in a randomised order, in the same session, with a 20-30minute break between sessions, until measured variables return to baseline. Participants will exercise with their arms supported at heart level and will be doing a high knees style aerobic exercise (similar to fast marching on the spot), with intensity monitored by a heart rate monitor (band across the chest and corresponding wrist watch), and VO2 (via mask) during the session. Participants will exercise for approximately 5 minutes at 40% of VO2 peak and 5 minutes at 60% of VO2 peak, before having a recovery period and seated rest for approximately 20-30 minutes, depending on baseline readings. After resting participants will take part in the same protocol for the other condition (wet or dry). Sessions will be supervised by a physiotherapist and exercise physiologist.

Sponsors

Curtin University
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

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

Inclusion criteria

* Stable, documented coronary heart disease and be at least 6 months following a myocardial infarction, coronary artery bypass graft or percutaneous coronary intervention *Have been taking stable medical therapy for the last 2 months *Be able to participate in exercise training 3 days per week and organise their own transport

Exclusion criteria

*Renal impairment, hepatic impairment, proteinurea or hyperuricaemia *Left ventricle ejection fraction below 45% *Musculoskeletal or neurological condition or injury that precludes exercise training *Any current or recent neoplasms or cancer treatment *Current smokers *Premenopausal females (due to the potential effects of hormonal cycle on vascular assessment) *Currently participating in a formal exercise program at least 3 times per week, or have done so in the last 6 weeks

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026