Cited by 10Cystic Fibrosis Research AdvancesNursing care and researchAdolescent and Pediatric Healthcare

The development and evaluation of a self-management program for cystic fibrosis

COTTRELL, CONSTANCE K., YOUNG, GORDON A., CREER, THOMAS L., HOLROYD, KENNETH A., KOTSES, HARRY·1996·Pediatric Asthma, Allergy & Immunology

Abstract

Cystic fibrosis (CF) is a major health concern with respect to morbidity and mortality. A self-management program was developed and evaluated to determine how such an approach might reduce the impact of CF on patients and their families. Despite constraints imposed by the context within which the investigation was conducted, positive findings were obtained. These results indicated that children who received self-management training showed significant improvement in weight gain, and aerosol and chest physiotherapy treatments. The conclusion was that self-management procedures should be considered as a major approach to take for improving the health and quality of life of CF patients and their families.

Integrity signals

Registry

Crossref · 10.1089/pai.1996.10.109

Cites

17 of 17 references verified0 citation errors · 0 not checkable

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  • Most included trials had small sample sizes; seven trials had fewer than 100 participants and many stated they were underpowered.

    “Most included trials had small sample sizes; seven trials had fewer than 100 participants and many stated they were underpowered (Cottrell 1996;Downs 2006;Gur 2016;Hind 2017;Knudsen 2016;Quinn 2004;Shakkottai 2017).”
  • Some included trials reported relatively large numbers of participants who had declined to take part, while others did not report this information at all.

    “Some of our included trials reported relatively large numbers of participants who had declined to take part (Cottrell 1996; Knudsen 2016; Wildman 2022); whilst others did not report this information at all.”
  • In two trials, the duration and intensity of the intervention was unclear.

    “In two trials, the duration and intensity of the intervention was unclear; either because no details were provided on the scheduling of the two six-hour training sessions (Cottrell 1996), or because it was unclear if the information provided (one clinic session and eight phone sessions over six months) was in reference to the intervention or active comparator arm, or both (Riekert 2013).”
  • 10 trials (69 references) were included in this review.

    “This leaves 10 trials (69 references) for inclusion in this review (Cottrell 1996;Downs 2006;Gur 2016;Hind 2017;Knudsen 2016;Quinn 2004;Quittner 2019;Riekert 2013;Shakkottai 2017;Wildman 2022).”
  • Nine of these 10 trials could also be included in limited quantitative syntheses (meta-analyses).

    “Nine of these 10 trials could also be included in limited quantitative syntheses (meta-analyses) (Cottrell 1996;Downs 2006;Gur 2016;Hind 2017;Knudsen 2016;Quinn 2004;Quittner 2019;Shakkottai 2017;Wildman 2022).”

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Authors
COTTRELL, C. K., YOUNG, G. A., CREER, T. L., HOLROYD, K. A., & KOTSES, H.
Venue
Pediatric Asthma, Allergy & Immunology
Published
1996-01
Volume
10
Issue
3
Pages
109-118
ISSN
  • 0883-1874 (ISSN-L)
  • 1557-7767
OpenAlex
W1993269239
Cited by
10
References
17
Citations by year
2023: 1 · 2021: 1 · 2019: 1 · 2018: 1 · 2017: 1 · 2016: 1 · 2014: 1
FWCI
0.00
Type
journal article
Language
en
Open access
closed
Locations
Pediatric Asthma Allergy & Immunology (publishedVersion)
Topics
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Cystic Fibrosis Research Advances
  • Health Sciences › Health Professions › Pharmacy › Nursing care and research
  • Health Sciences › Health Professions › Speech and Hearing › Adolescent and Pediatric Healthcare
Keywords
cystic fibrosis, self-management program, patient education, children, weight gain, inhalation therapy, chest physiotherapy, quality of life, family caregivers

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