Skip to content

Comparing an app-based breathing exercise program with standard breathing exercises in preparing breast cancer patients for breath-hold radiation therapy

A pilot randomised controlled trial assessing the feasibility and acceptability of a breathwork exercise program delivered via Physitrack, and its preliminary effects compared with standard departmental education, in patients undergoing deep inspiration breath hold radiotherapy.

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12626001055392
Enrollment
20
Registered
2026-08-26
Start date
2026-09-28
Completion date
2027-06-30
Last updated
2026-08-31

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 pilot study aims to assess the feasibility and acceptability of a structured breathwork exercise program delivered through the Physitrack mobile application for patients preparing to undergo Deep Inspiration Breath Hold (DIBH) radiation therapy. The study will investigate whether the program may help improve breathing control and breath-hold performance in patients who have difficulty performing DIBH because of respiratory limitations. Who is it for? You may be eligible for this study if you are male or female with a cancer diagnosis who have been offered DIBH radiation therapy but are unable to achieve or maintain adequate breath holds during initial assessment due to respiratory-related limitations. Participants must be able to provide informed consent and commence the program at least one week before their radiation therapy planning appointment. Study details Those who are eligible will be randomly assigned to one of two groups. One group will receive a structured breathwork exercise program delivered through the Physitrack mobile application, while the other group will receive the standard breath-hold exercises currently provided as part of routine departmental education. Participants in both groups will complete breathing exercises twice daily for approximately two weeks before their CT simulation/planning appointment, with each session taking less than 10 minutes. The intervention group will receive video-guided exercises, reminders, and adherence tracking through the Physitrack app, while the control group will receive written instructions and record exercise completion in a paper diary. Participants will undergo assessments of inspiratory capacity, breath-hold stability, and DIBH capability. Exercise adherence will also be monitored through app-recorded data or participant diaries, depending on group allocation. It is hoped that this research will determine whether a digital breathwork program is practical and acceptable for patients and provide information to support a larger trial aimed at improving access to and effectiveness of DIBH radiation therapy.

Interventions

What is the intervention? The intervention is a structured breathwork exercise program delivered through the Physitrack mobile application. The program uses exercises selected from the existing Physitrack exercise library to improve diaphragmatic breathing, respiratory control, and breath-hold performance in preparation for Deep Inspiration Breath Hold (DIBH) radiation therapy. Examples of these exercises include: diaphragmatic breathing, bilateral shoulder flexion with breathing, thoracic expan

What is the intervention? The intervention is a structured breathwork exercise program delivered through the Physitrack mobile application. The program uses exercises selected from the existing Physitrack exercise library to improve diaphragmatic breathing, respiratory control, and breath-hold performance in preparation for Deep Inspiration Breath Hold (DIBH) radiation therapy. Examples of these exercises include: diaphragmatic breathing, bilateral shoulder flexion with breathing, thoracic expansion, abdominal breathing and box breathing. The comparison group will receive the breath-hold exercises routinely provided as part of standard departmental education. Who delivers it and their relevant expertise? The exercise program will be prescribed by a Senior Exercise Physiologist with expertise in respiratory exercise prescription. The program will then be set up for the participant, who received the Physitrack arm, in the Physitrack application by the healthcare professional from the research team. The healthcare professional will either be the radiation therapist or radiation oncology nurse who obtained consent from the participant. This team member will also provide the participant with instructions on accessing and using the application. How is it delivered? The intervention is delivered individually through the Physitrack application. Participants receive video demonstrations, written instructions, exercise reminders, and adherence monitoring through the application. Participants allocated to the control arm receive standard departmental education and written instructions describing the breath-hold exercises. How often and for how long? Participants will complete the prescribed exercises twice daily for approximately two weeks before their CT simulation/planning appointment. Each session takes less than 10 minutes to complete and consists of four progressively challenging diaphragmatic breathing and breath-hold exercises designed to prepare patients for DIBH radiation therapy. Where is it delivered? Participants will be introduced to the intervention following their initial consultation with their radiation oncologist at the North Coast Cancer Institute, Lismore Base Hospital. The exercise program is then completed independently in the participant's home using the Physitrack application (intervention arm) or written exercise instructions (control arm). Adherence Participants allocated to the Physitrack arm will receive automated exercise reminders through the application, and adherence will be monitored using app-recorded exercise completion data. Both arm participants will record their exercise completion in a paper diary, which will be collected at their CT simulation appointment.

Sponsors

Northern NSW Local Health District
Lead SponsorGovernment body

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Educational / counselling / training
Masking
Open (masking not used)

Eligibility

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

Inclusion criteria

Patients with a diagnosis of cancer who have been offered Deep Inspiration Breath Hold (DIBH) radiation therapy. Unable to achieve or maintain adequate DIBH during the initial screening assessment due to respiratory-related limitations, verified using the department's respiratory monitoring system. Able to provide informed written consent. Able to commence the intervention at least one week before their computed tomography simulation/planning appointment.

Exclusion criteria

Able to achieve and maintain adequate deep inspiration breath hold during the initial screening assessment. Unable to perform deep inspiration breath hold for reasons unrelated to respiratory limitations, such as pain, anxiety, or difficulty maintaining the treatment position. Medical contraindication to undertaking the prescribed breathing exercises. Unable to understand the study materials or use the Physitrack program without appropriate language support. Less than one week between consent and the computed tomography simulation/planning appointment.

Outcome results

None listed

Source: ANZCTR · Data processed: Sep 19, 2026