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. 2019 Jan 24;19(1):21.
doi: 10.1186/s12890-019-0784-z.

CyFiT telehealth: protocol for a randomised controlled trial of an online outpatient physiotherapy service for children with cystic fibrosis

Affiliations

CyFiT telehealth: protocol for a randomised controlled trial of an online outpatient physiotherapy service for children with cystic fibrosis

Ray Lei Lang et al. BMC Pulm Med. .

Abstract

Background: Telehealth and telemonitoring is an emerging area of study in people with cystic fibrosis (CF), with the potential of increasing access to care, and minimising infection control risks to patients without compromising their health outcomes. To date, limited evidence is available to support the use of telehealth in paediatric population with CF in a clinical setting. This study aims to investigate the utility of a multimodal telehealth-based outpatient physiotherapy service and assess its effect on quality of life, functional exercise capacity, hospital admission and intravenous antibiotic requirements, lung function, processes of care, participation in activities of daily living, and health economics associated with operating an innovative service.

Method: This single centre, prospective, parallel, randomised, controlled, non-inferiority trial aims to recruit 110 children with CF between the ages 8 to 18 years of age. Participants will be randomised to the Usual Outpatient Physiotherapy Service group (Usual OPS) or the telehealth intervention group (CyFiT OPS). Quality of life, participation in activity of daily living, functional exercise capacity and patient perception of care will be examined every six months using the Cystic Fibrosis Questionnaire-Revised (CFQ-R), Children's Assessment of Participation and Enjoyment (CAPE), Preferences for Activities of Children (PAC) questionnaire, Modified Shuttle Test-25 (MST25), and Measure of Process of Care (MPOC-20) questionnaire. Physiological measurements collected during routine clinical visits such as spirometry, body weight and height, information will be retrospectively retrieved via a chart review at the end of the study.

Discussion: We anticipate that this multi-modal telehealth service will deliver a comparable service to traditional face-to-face models. An alternative to existing outpatient physiotherapy services may potentially increase patient options for access to care and patient-orientated outcomes such as quality of life. If deemed appropriate, the new model of care can be integrated into clinical practice immediately.

Trial registration: This trial is registered with the Australian and New Zealand Clinical Trial Registry ( ACTRN12617001035314 ) last updated 17th July 2018.

Keywords: Children; Cystic fibrosis; Health economics; Physical activity; Telehealth; Telemonitoring.

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Conflict of interest statement

Ethics approval and consent to participate

This study has been registered with the Australian and New Zealand Clinical Trial Registry (Trial ID: ACTRN12617001035314).

Ethics approval has been obtained from the Children’s Health Queensland Hospital and Health Service (CHQ-HHS) (approval number: HREC/17/QRCH/124) and The University of Queensland (approval number: 2017001073/HREC/17/QRCH/124).

Written consent will be obtained by parents or legal guardians of children between the ages 8 to 18 years wishing to participate in the study. Concurrently, written assent will be obtained from children.

Consent for publication

Participants will provide written consent for their data to be used in publication. Further written consent will be gained by participants in deidentified images will be used in publication.

Competing interests

One author TR has a material interest in the eHAB telerehabilitation system used in this study. This author will not be involved in the collection or analysis of study data. The remaining authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Figures

Fig. 1
Fig. 1
Integration of CyFiT Intervention with current Model of Care

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References

    1. Button BM, Wilson C, Dentice R, Cox NS, Middleton A, Tannenbaum E, et al. Physiotherapy for cystic fibrosis in Australia and New Zealand: a clinical practice guideline. Respirology. 2016;21(4):656–667. doi: 10.1111/resp.12764. - DOI - PMC - PubMed
    1. Arias Llorente RP, Bousono Garcia C, Diaz Martin JJ. Treatment compliance in children and adults with cystic fibrosis. J Cyst Fibros. 2008;7(5):359–367. doi: 10.1016/j.jcf.2008.01.003. - DOI - PubMed
    1. Passero MA, Remor B, Salomon J. Patient-reported compliance with cystic fibrosis therapy. Clin Pediatr (Phila) 1981;20(4):264–268. doi: 10.1177/000992288102000406. - DOI - PubMed
    1. Sawicki GS, Ren CL, Konstan MW, Millar SJ, Pasta DJ, Quittner AL. Treatment complexity in cystic fibrosis: trends over time and associations with site-specific outcomes. J Cyst Fibros. 2013;12(5):461–467. doi: 10.1016/j.jcf.2012.12.009. - DOI - PMC - PubMed
    1. Tagliente I, Solvoll T, Trieste L, De Cecco CN, Murgia F, Bella S. Which indicators for measuring the daily physical activity? An overview on the challenges and technology limits for telehealth applications. Technol Health Care. 2016;24(5):665–672. doi: 10.3233/thc-161216. - DOI - PubMed

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