Quality of life · people with dermatomyositis and polymyositis
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Quality of life · boys with DMD
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Quality of life · people with facioscapulohumeral muscular dystrophy
1 finding from 1 review
no estimate extracted
Studies not reported
Low
Quality of life · people with mitochondrial myopathy
1 finding from 1 review
no estimate extracted
Studies not reported
Very low
Quality of life · people with myotonic dystrophy type 1
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Quality of life · people with dermatomyositis and polymyositis
1 finding from 1 review
no estimate extracted
Studies not reported
Very low
Quality of life · people with facioscapulohumeral muscular dystrophy
1 finding from 1 review
no estimate extracted
Studies not reported
Very low
Quality of life · children and adolescents with juvenile dermatomyositis
1 finding from 1 review
no estimate extracted
Studies not reported
Low
Quality of life (SF‐12 PCS) · people with NMD
1 finding from 1 review
Quality of life (SF‐12 MCS) · people with NMD
1 finding from 1 review
Quality of life In children, · children and adults with SMA type 3
1 finding from 1 review
Quality of life · participants with limb‐girdle muscular dystrophy or Becker muscular dystrophy
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Quality of life · people with myasthenia gravis
1 finding from 1 review
Quality of life · people with facioscapulohumeral muscular dystrophy
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Quality of life · people with myotonic dystrophy
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Long‐term improvement in functional ability or health‐related quality of life (more than three months) · People with carpal tunnel syndrome on a waiting list for carpal tunnel release
1 finding from 1 review
Short‐term improvement in functional ability or health‐related quality of life (hand function) (three months or less) · People with carpal tunnel syndrome on a waiting list for carpal tunnel release
It is very uncertain whether neurodynamic mobilisation changes short‐term improvement in functional ability or health‐related… compared with no treatment (very low certainty).
1 finding from 1 review