Literature DB >> 12527601

Questions on life satisfaction for adolescents and adults with cystic fibrosis: development of a disease-specific questionnaire.

Lutz Goldbeck1, Tim G Schmitz, Gerhard Henrich, Peter Herschbach.   

Abstract

STUDY
OBJECTIVES: The development and psychometric properties of an additional disease-specific module of the Questions on Life Satisfaction for adolescents and adults with cystic fibrosis (FLZ(M)-CF) are described. The Questions on Life Satisfaction (FLZ(M)) instrument allows the respondent to rate the subjective importance and her/his satisfaction with different domains of life.
METHODS: A preliminary 16-item version of the scale was employed in a study with 243 German patients with cystic fibrosis (CF) [16 to 58 years of age; FEV(1), 15 to 121% of predicted], together with the "general life satisfaction" module and the "satisfaction with health" module of the FLZ(M). Item elimination according to the principle of least common variance resulted in the final nine-item version.
RESULTS: Cronbach alpha for the FLZ(M)-CF was 0.80; the split-half reliability was 0.72. Convergent validity of the scale was indicated by Pearson correlations of r = 0.75 with the generic satisfaction with health scale of the FLZ(M), r = 0.30 with FEV(1)%, and r = - 0.26 with daily time for home therapy. The scale discriminated significantly between patients with and without need for assistance in daily life and between patients with and without a partner.
CONCLUSIONS: The FLZ(M)-CF is a reliable and valid instrument, and it is short enough to be used as screening instrument. The combination of generic and disease-specific scales within the FLZ(M) allows comprehensive measurement of life satisfaction for patients with CF who are > 15 years old.

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Year:  2003        PMID: 12527601     DOI: 10.1378/chest.123.1.42

Source DB:  PubMed          Journal:  Chest        ISSN: 0012-3692            Impact factor:   9.410


  10 in total

1.  Validity and Reliability of a Novel Multimodal Questionnaire for the Assessment of Abdominal Symptoms in People with Cystic Fibrosis (CFAbd-Score).

Authors:  Anke Jaudszus; Elisa Zeman; Tatjana Jans; Elena Pfeifer; Harold Tabori; Christin Arnold; Ruth K Michl; Michael Lorenz; Natalie Beiersdorf; Jochen G Mainz
Journal:  Patient       Date:  2019-08       Impact factor: 3.883

2.  Growing up with cystic fibrosis: achievement, life satisfaction, and mental health.

Authors:  Tanja Besier; Lutz Goldbeck
Journal:  Qual Life Res       Date:  2012-01-04       Impact factor: 4.147

3.  Life-space mobility is associated with frequency of hospitalization in adults with cystic fibrosis.

Authors:  Eric Raphael Gottlieb; Elisabeth Christine Smith; Linda Lucetta Wolfenden; Richard Mark Allman; Vin Tangpricha
Journal:  Clin Respir J       Date:  2010-10-01       Impact factor: 2.570

4.  Reliability and validity of the Cystic Fibrosis Questionnaire-Revised for children and parents in Turkey: cross-sectional study.

Authors:  Hasan Yuksel; Ozge Yilmaz; Deniz Dogru; Bulent Karadag; Fatih Unal; Alexandra L Quittner
Journal:  Qual Life Res       Date:  2012-04-11       Impact factor: 4.147

Review 5.  Measuring and improving respiratory outcomes in cystic fibrosis lung disease: opportunities and challenges to therapy.

Authors:  Edith T Zemanick; J Kirk Harris; Steven Conway; Michael W Konstan; Bruce Marshall; Alexandra L Quittner; George Retsch-Bogart; Lisa Saiman; Frank J Accurso
Journal:  J Cyst Fibros       Date:  2009-10-14       Impact factor: 5.482

6.  The effect of inpatient rehabilitation programmes on quality of life in patients with cystic fibrosis: a multi-center study.

Authors:  Tim G Schmitz; Lutz Goldbeck
Journal:  Health Qual Life Outcomes       Date:  2006-02-03       Impact factor: 3.186

7.  Higher mobility scores in patients with cystic fibrosis are associated with better lung function.

Authors:  Aneesha Thobani; Jessica A Alvarez; Shaina Blair; Kaila Jackson; Eric R Gottlieb; Seth Walker; Vin Tangpricha
Journal:  Pulm Med       Date:  2015-02-18

8.  The Cystic Fibrosis Impact Questionnaire: qualitative development and cognitive evaluation of a new patient-reported outcome instrument to assess the life impacts of cystic fibrosis.

Authors:  Kelly P McCarrier; Mariam Hassan; Paul Hodgkins; Ellison Suthoff; Lisa J McGarry; Mona L Martin
Journal:  J Patient Rep Outcomes       Date:  2020-05-13

9.  Health-related quality of life in children with cystic fibrosis: validation of the German CFQ-R.

Authors:  Anne Schmidt; Kerstin Wenninger; Nadja Niemann; Ulrich Wahn; Doris Staab
Journal:  Health Qual Life Outcomes       Date:  2009-12-02       Impact factor: 3.186

10.  Assessment of a Mobile App by Adolescents and Young Adults With Cystic Fibrosis: Pilot Evaluation.

Authors:  Isa Rudolf; Katharina Pieper; Helga Nolte; Sibylle Junge; Christian Dopfer; Annette Sauer-Heilborn; Felix C Ringshausen; Burkhard Tümmler; Ute von Jan; Urs-Vito Albrecht; Jan Fuge; Gesine Hansen; Anna-Maria Dittrich
Journal:  JMIR Mhealth Uhealth       Date:  2019-11-21       Impact factor: 4.773

  10 in total

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