Literature DB >> 23797564

The development and validation of the Family Reported Outcome Measure (FROM-16)© to assess the impact of disease on the partner or family member.

Catherine Jane Golics, Mohammad Khurshid Azam Basra, Andrew Yule Finlay, Sam Salek.   

Abstract

PURPOSE: The impact of patients’ illness on family members has proven to be both widespread and severe. Currently, there is no generic instrument that can be used to measure the impact of illnesses on the partner or family members of patients. This study describes the development of the Family Reported Outcome Measure (FROM-16)©.
METHODS: A total of 30 items were generated from the content of previous interviews with family members. Qualitative and quantitative feedback from expert panels was collected. Items were reduced using both Rasch analysis and factor analysis, and full psychometric testing was carried out including construct validity and reliability.
RESULTS: Collapsing response categories, removing misfitting items and combining residually correlating items produced a good fit to the Rasch model (n = 240, total χ2 = 56.6, df = 48, p = 0.18). Factor analysis produced a 16-item measure with two factors. The FROM showed high internal consistency (n = 120, Cronbach’s α = 0.80–0.89), high reproducibility (n = 51, intraclass correlation = 0.85–0.92) and a mean completion time of 2 min. Construct validity was proven through the correlation between the FROM and the WHOQOL-BREF total scores (n = 119, r = −0.53–0.52, p < 0.001), and the correlation between the FROM and the patient’s overall health score (n = 120, r = −0.45–0.48, p < 0.001).
CONCLUSION: The FROM-16 is both reliable and valid for use. It has a potential for wide use, including clinical (healthcare professionals or researchers in all medical specialties), industrial and social sciences. The FROM can be used to identify areas where family members need further support, as well as identify those individuals most affected by the patient’s illness.

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Year:  2014        PMID: 23797564     DOI: 10.1007/s11136-013-0457-y

Source DB:  PubMed          Journal:  Qual Life Res        ISSN: 0962-9343            Impact factor:   4.147


  22 in total

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Review 9.  The impact of disease on family members: a critical aspect of medical care.

Authors:  Catherine Jane Golics; Mohammad Khurshid Azam Basra; Andrew Yule Finlay; Sam Salek
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  8 in total

1.  Family Reported Outcome Measure - 16 (FROM-16): Creation, Reliability and Reproducibility of the Polish Language Version.

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2.  Validation of the Thai version of the family reported outcome measure (FROM-16)© to assess the impact of disease on the partner or family members of patients with cancer.

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4.  Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS): Major Impact on Lives of Both Patients and Family Members.

Authors:  Esme Brittain; Nina Muirhead; Andrew Y Finlay; Jui Vyas
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5.  Validation of the German version of the Family Reported Outcome Measure (FROM-16) to assess the impact of disease on the partner or family member.

Authors:  Susanne A Elsner; Sam S Salek; Andrew Y Finlay; Anna Hagemeier; Catherine J Bottomley; Alexander Katalinic; Annika Waldmann
Journal:  Health Qual Life Outcomes       Date:  2021-03-24       Impact factor: 3.186

6.  Impact of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) on the quality of life of people with ME/CFS and their partners and family members: an online cross-sectional survey.

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Review 7.  Counting the Burden: Atopic Dermatitis and Health-related Quality of Life.

Authors:  Faraz Ali; Jui Vyas; Andrew Y Finlay
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8.  Appraisal of patient-reported outcome measures in analogous diseases and recommendations for use in phase II and III clinical trials of pyruvate kinase deficiency.

Authors:  M S Salek; T Ionova; J R Johns; E N Oliva
Journal:  Qual Life Res       Date:  2018-11-19       Impact factor: 4.147

  8 in total

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