Table 5.
Patient-reported outcome measures that are used in MS research
| Measure |
|---|
| Quality of life |
| MS Quality of Life-54 [103] |
| MS Quality of Life Inventory [86] |
| European Quality of Life-5D [87] |
| Health Utilities Index Mark 3 [87] |
| World Health Organization Quality of Life Brief Form [100] |
| Sickness Impact Profile [83] |
| Life Satisfaction Questionnaire [96] |
| Hamburg Quality of Life Questionnaire in MS [91] |
| Quality of Life Index [85] |
| Leeds MS Quality of Life Scale [90] |
| Disability and Impact Profile [101] |
| The MS International Quality of Life Questionnaire [102] |
| Functional Assessment of MS [84] |
| Depression and anxiety |
| Beck Depression Inventory [82] |
| Patient Health Questionnaire-9 [95] |
| Hospital Anxiety and Depression Scale [94] |
| Fatigue |
| Modified Fatigue Impact Scale [89] |
| Fatigue Impact Scale for Daily Use [88] |
| Single functional domain |
| MS Walking Scale-12 [93] |
| Arm Function in MS Questionnaire [98] |
| Visual Function Questionnaire-25 [99] |
| Multiple domains |
| Short Form-36 [104] |
| MS Impact Scale-29 [92] |
| Guy’s Neurological Disability Scale [97] |
| MS Impact Profile [105] |
MS Multiple sclerosis