Abstract
Background: Patient-reported outcomes are important for clinical research and care, yet administering and scoringthe questionnaires requires considerable effort and time. The Patient Reported Outcomes Measurement InformationSystem (PROMIS) could considerably reduce administrative obstacles and lessen survey burden for participants.Objective: Assess the feasibility and validity of PROMIS, compared to commonly-used legacy measures for multiplesclerosis (MS).Methods: In this cross-sectional survey, 133 participants with confirmed MS completed legacy surveys and PROMISComputerized Adaptive Tests (CATs) for depression, anxiety, pain, fatigue and physical function. We conducted a multitrait,multi-method analysis and verified results with confirmatory factor analysis.Results: The correlations between PROMIS and the corresponding legacy measures were large (0.67 to 0.87). Themulti-trait, multi-method criteria were generally well met, providing good evidence of the validity of PROMIS measures.PROMIS surveys asked fewer questions and required substantially less time to complete than the legacy scales.Conclusions: Our results provide evidence of the construct validity of PROMIS for use with MS patients. Severalaspects of the PROMIS CATs made them an important resource, including: (a) less time was required to complete them;(b) missing data was reduced; and (c) the automatic scoring referenced the general population. Our findings support theuse of PROMIS in MS research and may have broader implications for clinical care, as well.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 1102-1111 |
| Number of pages | 10 |
| Journal | Multiple Sclerosis |
| Volume | 20 |
| Issue number | 8 |
| DOIs | |
| State | Published - 2014 |
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Keywords
- Computerized Adaptive Test
- multiple sclerosis
- outcome measurement
- PROMIS
- self-reporting
- survey design
- validation
ASJC Scopus subject areas
- Clinical Neurology
- Neurology
Cite this
Reducing survey burden : Feasibility and validity of PROMIS measures in multiple sclerosis. / Senders, Angela; Hanes, Douglas; Bourdette, Dennis; Whitham, Ruth; Shinto, Lynne.
In: Multiple Sclerosis, Vol. 20, No. 8, 2014, p. 1102-1111.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Reducing survey burden
T2 - Feasibility and validity of PROMIS measures in multiple sclerosis
AU - Senders, Angela
AU - Hanes, Douglas
AU - Bourdette, Dennis
AU - Whitham, Ruth
AU - Shinto, Lynne
PY - 2014
Y1 - 2014
N2 - Background: Patient-reported outcomes are important for clinical research and care, yet administering and scoringthe questionnaires requires considerable effort and time. The Patient Reported Outcomes Measurement InformationSystem (PROMIS) could considerably reduce administrative obstacles and lessen survey burden for participants.Objective: Assess the feasibility and validity of PROMIS, compared to commonly-used legacy measures for multiplesclerosis (MS).Methods: In this cross-sectional survey, 133 participants with confirmed MS completed legacy surveys and PROMISComputerized Adaptive Tests (CATs) for depression, anxiety, pain, fatigue and physical function. We conducted a multitrait,multi-method analysis and verified results with confirmatory factor analysis.Results: The correlations between PROMIS and the corresponding legacy measures were large (0.67 to 0.87). Themulti-trait, multi-method criteria were generally well met, providing good evidence of the validity of PROMIS measures.PROMIS surveys asked fewer questions and required substantially less time to complete than the legacy scales.Conclusions: Our results provide evidence of the construct validity of PROMIS for use with MS patients. Severalaspects of the PROMIS CATs made them an important resource, including: (a) less time was required to complete them;(b) missing data was reduced; and (c) the automatic scoring referenced the general population. Our findings support theuse of PROMIS in MS research and may have broader implications for clinical care, as well.
AB - Background: Patient-reported outcomes are important for clinical research and care, yet administering and scoringthe questionnaires requires considerable effort and time. The Patient Reported Outcomes Measurement InformationSystem (PROMIS) could considerably reduce administrative obstacles and lessen survey burden for participants.Objective: Assess the feasibility and validity of PROMIS, compared to commonly-used legacy measures for multiplesclerosis (MS).Methods: In this cross-sectional survey, 133 participants with confirmed MS completed legacy surveys and PROMISComputerized Adaptive Tests (CATs) for depression, anxiety, pain, fatigue and physical function. We conducted a multitrait,multi-method analysis and verified results with confirmatory factor analysis.Results: The correlations between PROMIS and the corresponding legacy measures were large (0.67 to 0.87). Themulti-trait, multi-method criteria were generally well met, providing good evidence of the validity of PROMIS measures.PROMIS surveys asked fewer questions and required substantially less time to complete than the legacy scales.Conclusions: Our results provide evidence of the construct validity of PROMIS for use with MS patients. Severalaspects of the PROMIS CATs made them an important resource, including: (a) less time was required to complete them;(b) missing data was reduced; and (c) the automatic scoring referenced the general population. Our findings support theuse of PROMIS in MS research and may have broader implications for clinical care, as well.
KW - Computerized Adaptive Test
KW - multiple sclerosis
KW - outcome measurement
KW - PROMIS
KW - self-reporting
KW - survey design
KW - validation
UR - http://www.scopus.com/inward/record.url?scp=84904816643&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84904816643&partnerID=8YFLogxK
U2 - 10.1177/1352458513517279
DO - 10.1177/1352458513517279
M3 - Article
C2 - 24402035
AN - SCOPUS:84904816643
VL - 20
SP - 1102
EP - 1111
JO - Multiple Sclerosis
JF - Multiple Sclerosis
SN - 1352-4585
IS - 8
ER -