| Literature DB >> 15169564 |
Philip Moons1, Kristel Marquet, Werner Budts, Sabina De Geest.
Abstract
BACKGROUND: The 'Schedule for the Evaluation of Individual Quality of Life-Direct Weighting' (SEIQoL-DW) is an instrument developed to measure individual quality of life. Although this instrument has been used in numerous studies, data on validity and reliability are sparse. This study aimed to examine aspects of validity, reliability and responsiveness of the SEIQoL-DW on data obtained in adults with congenital heart disease, by using the new standards of psychological testing.Entities:
Mesh:
Year: 2004 PMID: 15169564 PMCID: PMC434529 DOI: 10.1186/1477-7525-2-27
Source DB: PubMed Journal: Health Qual Life Outcomes ISSN: 1477-7525 Impact factor: 3.186
Research questions (Q) and hypotheses (H) to provide evidence on validity and reliability of the SEIQoL-DW
| Q1: Does the SEIQoL-DW measure quality of life, given the new conceptualization? |
| Q2: In how many patients are the responses on the SEIQoL-DW invalid? |
| Q3: What is the percentage of positive and negative domains nominated by the patients? |
| H1: There is a low to moderate correlation between the scores of the actual status and the relative importance. |
| H2: There is a high correlation between the scores of the actual status in patients who reported |
| H3: There is a lower score in the actual status of |
| H4: There is a lower score in the actual status of |
| H5: There is a lower score in the actual status of |
| H6: There is a low to moderate correlation between the SEIQoL-DW index score and the linear analog scale of quality of life. |
| H7: The SEIQoL-DW index score remains stable in patients in whom no medical or psychosocial changes occur during an interval of one year. |
| H8: Changes in the scores of the actual status in patients who reported |
| H9: Changes in health status are not or marginally correlated with changes in SEIQoL-DW index score. |
| Q4: What is the percentage of patients with the lowest (0 = floor) and highest possible score (100 = ceiling) on the SEIQoL-DW index? |
Characteristics of adults with congenital heart disease included in the cross-sectional and longitudinal study
| Gender: | NS | ||
| Male | 347 (59.9%) | 78 (60%) | |
| Female | 232 (40.1%) | 52 (40%) | |
| Median age (in years) | 23 (Q1 = 20; Q3 = 29) | 24 (Q1 = 21; Q3 = 29) | NS |
| Marital status: | NS | ||
| Unmarried (living with parents) | 324 (55.9%) | 70 (53.8%) | |
| Living alone, divorced or widowed | 56 (9.7%) | 14 (10.8%) | |
| Married or cohabiting | 199 (34.4%) | 46 (35.4%) | |
| Highest educational level: | NS | ||
| Vocational high school | 188 (32.5%) | 45 (34.6%) | |
| (Technical) high school | 127 (21.9%) | 27 (20.8%) | |
| College/University | 245 (42.3%) | 52 (39.9%) | |
| Other | 19 (3.3%) | 6 (4.7%) | |
| Employment status: | NS | ||
| Student | 167 (28.8%) | 34 (26.2%) | |
| Employed | 342 (59.1%) | 78 (60.0%) | |
| Unemployed/Looking for work | 19 (3.3%) | 7 (5.4%) | |
| Not able to work/Disability | 15 (2.6%) | 5 (3.8%) | |
| Other | 36 (6.2%) | 6 (4.6%) | |
| Median frequency of follow-up at the Adult Congenital Heart Clinic (in years) | 1.5 (Q1 = 1.0; Q3 = 3.0) | 1.0 (Q1 = 1.0; Q3 = 1.0) | U = 18713 p < 0.001 |
NS= not significant