NCT01721044 · OUTCOME
Change From Baseline in Mental Component Score (MCS), Physical Component Score (PCS) of the Medical Outcomes Study 36-Item Short Form Health Survey Version 2 Acute (SF-36v2 Acute)
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- MEAN
- Unit
- Units on a Scale
- Interval / dispersion
- Standard Deviation
- Time frame
- Baseline, Week 12, Week 24
What was measured
The SF-36 is a health-related survey that assesses participant's quality of life and consists of 36 questions covering 8 health domains: physical functioning, bodily pain, role limitations due to physical problems and emotional problems, general health, mental health, social functioning, vitality, and 2 component scores (mental \[MCS\] and physical \[PCS\]). MCS consisted of social functioning, vitality, mental health, and role-emotional scales. PCS consisted of physical functioning, bodily pain, role-physical, and general health scales. Each domain is scored by summing the individual items and transforming the scores into a 0 to 100 scale with higher scores indicating better health status.
Analysis population: mITT population includes all randomized participants who received at least 1 dose of the study drug. Participants were analyzed according to the study drug to which they were randomized. Missing values due to discontinuation of study or drug, rescue, or missing data were imputed using NRI.
Groups in this outcome
Placebo
Placebo administered PO QD through Week 24. Participants continued to take background cDMARD therapy throughout study.
Baricitinib 2 mg
Baricitinib 2 mg administered PO QD through Week 24. Participants continued to take background cDMARD therapy throughout study.
Baricitinib 4 mg
Baricitinib 4 mg administered PO QD through Week 24. Participants continued to take background cDMARD therapy throughout study.
| Group | Source count |
|---|---|
| Placebo | 168 |
| Baricitinib 2 mg | 168 |
| Baricitinib 4 mg | 174 |
Reported measurements
Week 12 MCS
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Placebo | 1.6 | 10.7 | Not reported | Not reported | Not reported |
| Baricitinib 2 mg | 3.4 | 9.7 | Not reported | Not reported | Not reported |
| Baricitinib 4 mg | 2.4 | 10.0 | Not reported | Not reported | Not reported |
Week 24 MCS
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Placebo | 2.5 | 10.8 | Not reported | Not reported | Not reported |
| Baricitinib 2 mg | 3.2 | 11.5 | Not reported | Not reported | Not reported |
| Baricitinib 4 mg | 3.3 | 10.6 | Not reported | Not reported | Not reported |
Week 12 PCS
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Placebo | 3.3 | 8.0 | Not reported | Not reported | Not reported |
| Baricitinib 2 mg | 6.3 | 8.8 | Not reported | Not reported | Not reported |
| Baricitinib 4 mg | 6.4 | 8.8 | Not reported | Not reported | Not reported |
Week 24 PCS
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Placebo | 2.4 | 8.2 | Not reported | Not reported | Not reported |
| Baricitinib 2 mg | 6.4 | 8.9 | Not reported | Not reported | Not reported |
| Baricitinib 4 mg | 7.0 | 9.3 | Not reported | Not reported | Not reported |
Source statistical analyses
- ci Num Sides
- TWO_SIDED
- group Description
- MCS Week 12
- group Ids
- OG000
- OG002
- non Inferiority Type
- SUPERIORITY_OR_OTHER_LEGACY
- p Value
- 0.448
- statistical Method
- ANCOVA
- ci Num Sides
- TWO_SIDED
- group Description
- MCS Week 12
- group Ids
- OG000
- OG001
- non Inferiority Type
- SUPERIORITY_OR_OTHER_LEGACY
- p Value
- 0.058
- statistical Method
- ANCOVA
- ci Num Sides
- TWO_SIDED
- group Description
- MCS Week 24
- group Ids
- OG000
- OG002
- non Inferiority Type
- SUPERIORITY_OR_OTHER_LEGACY
- p Value
- 0.446
- statistical Method
- ANCOVA
- ci Num Sides
- TWO_SIDED
- group Description
- MCS Week 24
- group Ids
- OG000
- OG001
- non Inferiority Type
- SUPERIORITY_OR_OTHER_LEGACY
- p Value
- 0.401
- statistical Method
- ANCOVA
- ci Num Sides
- TWO_SIDED
- group Description
- PCS Week 12
- group Ids
- OG000
- OG002
- non Inferiority Type
- SUPERIORITY_OR_OTHER_LEGACY
- p Value
- 0.001
- statistical Method
- ANCOVA
- ci Num Sides
- TWO_SIDED
- group Description
- PCS Week 12
- group Ids
- OG000
- OG001
- non Inferiority Type
- SUPERIORITY_OR_OTHER_LEGACY
- p Value
- 0.001
- statistical Method
- ANCOVA
- ci Num Sides
- TWO_SIDED
- group Description
- PCS Week 24
- group Ids
- OG000
- OG002
- non Inferiority Type
- SUPERIORITY_OR_OTHER_LEGACY
- p Value
- 0.001
- statistical Method
- ANCOVA
- ci Num Sides
- TWO_SIDED
- group Description
- PCS Week 24
- group Ids
- OG000
- OG001
- non Inferiority Type
- SUPERIORITY_OR_OTHER_LEGACY
- p Value
- 0.001
- statistical Method
- ANCOVA
Complete source fields
- analyses
- ci Num Sides
- TWO_SIDED
- group Description
- MCS Week 12
- group Ids
- OG000
- OG002
- non Inferiority Type
- SUPERIORITY_OR_OTHER_LEGACY
- p Value
- 0.448
- statistical Method
- ANCOVA
- ci Num Sides
- TWO_SIDED
- group Description
- MCS Week 12
- group Ids
- OG000
- OG001
- non Inferiority Type
- SUPERIORITY_OR_OTHER_LEGACY
- p Value
- 0.058
- statistical Method
- ANCOVA
- ci Num Sides
- TWO_SIDED
- group Description
- MCS Week 24
- group Ids
- OG000
- OG002
- non Inferiority Type
- SUPERIORITY_OR_OTHER_LEGACY
- p Value
- 0.446
- statistical Method
- ANCOVA
- ci Num Sides
- TWO_SIDED
- group Description
- MCS Week 24
- group Ids
- OG000
- OG001
- non Inferiority Type
- SUPERIORITY_OR_OTHER_LEGACY
- p Value
- 0.401
- statistical Method
- ANCOVA
- ci Num Sides
- TWO_SIDED
- group Description
- PCS Week 12
- group Ids
- OG000
- OG002
- non Inferiority Type
- SUPERIORITY_OR_OTHER_LEGACY
- p Value
- 0.001
- statistical Method
- ANCOVA
- ci Num Sides
- TWO_SIDED
- group Description
- PCS Week 12
- group Ids
- OG000
- OG001
- non Inferiority Type
- SUPERIORITY_OR_OTHER_LEGACY
- p Value
- 0.001
- statistical Method
- ANCOVA
- ci Num Sides
- TWO_SIDED
- group Description
- PCS Week 24
- group Ids
- OG000
- OG002
- non Inferiority Type
- SUPERIORITY_OR_OTHER_LEGACY
- p Value
- 0.001
- statistical Method
- ANCOVA
- ci Num Sides
- TWO_SIDED
- group Description
- PCS Week 24
- group Ids
- OG000
- OG001
- non Inferiority Type
- SUPERIORITY_OR_OTHER_LEGACY
- p Value
- 0.001
- statistical Method
- ANCOVA
- classes
- categories
- measurements
- group Id
- OG000
- spread
- 10.7
- value
- 1.6
- group Id
- OG001
- spread
- 9.7
- value
- 3.4
- group Id
- OG002
- spread
- 10.0
- value
- 2.4
- title
- Week 12 MCS
- categories
- measurements
- group Id
- OG000
- spread
- 10.8
- value
- 2.5
- group Id
- OG001
- spread
- 11.5
- value
- 3.2
- group Id
- OG002
- spread
- 10.6
- value
- 3.3
- title
- Week 24 MCS
- categories
- measurements
- group Id
- OG000
- spread
- 8.0
- value
- 3.3
- group Id
- OG001
- spread
- 8.8
- value
- 6.3
- group Id
- OG002
- spread
- 8.8
- value
- 6.4
- title
- Week 12 PCS
- categories
- measurements
- group Id
- OG000
- spread
- 8.2
- value
- 2.4
- group Id
- OG001
- spread
- 8.9
- value
- 6.4
- group Id
- OG002
- spread
- 9.3
- value
- 7.0
- title
- Week 24 PCS
- denoms
- counts
- group Id
- OG000
- value
- 168
- group Id
- OG001
- value
- 168
- group Id
- OG002
- value
- 174
- units
- Participants
- description
- The SF-36 is a health-related survey that assesses participant's quality of life and consists of 36 questions covering 8 health domains: physical functioning, bodily pain, role limitations due to physical problems and emotional problems, general health, mental health, social functioning, vitality, and 2 component scores (mental \[MCS\] and physical \[PCS\]). MCS consisted of social functioning, vitality, mental health, and role-emotional scales. PCS consisted of physical functioning, bodily pain, role-physical, and general health scales. Each domain is scored by summing the individual items and transforming the scores into a 0 to 100 scale with higher scores indicating better health status.
- dispersion Type
- Standard Deviation
- groups
- description
- Placebo administered PO QD through Week 24. Participants continued to take background cDMARD therapy throughout study.
- id
- OG000
- title
- Placebo
- description
- Baricitinib 2 mg administered PO QD through Week 24. Participants continued to take background cDMARD therapy throughout study.
- id
- OG001
- title
- Baricitinib 2 mg
- description
- Baricitinib 4 mg administered PO QD through Week 24. Participants continued to take background cDMARD therapy throughout study.
- id
- OG002
- title
- Baricitinib 4 mg
- param Type
- MEAN
- population Description
- mITT population includes all randomized participants who received at least 1 dose of the study drug. Participants were analyzed according to the study drug to which they were randomized. Missing values due to discontinuation of study or drug, rescue, or missing data were imputed using NRI.
- reporting Status
- POSTED
- time Frame
- Baseline, Week 12, Week 24
- title
- Change From Baseline in Mental Component Score (MCS), Physical Component Score (PCS) of the Medical Outcomes Study 36-Item Short Form Health Survey Version 2 Acute (SF-36v2 Acute)
- type
- SECONDARY
- unit Of Measure
- Units on a Scale
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