Intervention not reported
Diastolic blood pressure clinical digital sphygmomanometer · adults with or without hypertension
1 finding from 1 review
Intervention not reported
Withdrawals due to adverse effects · adults with or without hypertension
1 finding from 1 review
Intervention not reported
Proportion of participants with IOP < 21 mmHg at 1 year' · participants with glaucoma or ocular hypertension
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Intervention not reported
Mean IOP change from baseline at 1 year' · participants with glaucoma or ocular hypertension
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Intervention not reported
Participant‐reported outcomes related to the ease, convenience, and comfort of instillation at 1 year' · participants with glaucoma or ocular hypertension
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Intervention not reported
Physiologic measurements of systemic absorption at 1 year' · participants with glaucoma or ocular hypertension
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Intervention not reported
Escalation of therapy at 1 year' · participants with glaucoma or ocular hypertension
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Intervention not reported
Mean change in visual fields at 1 year' · participants with glaucoma or ocular hypertension
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Intervention not reported
Adverse events at 1 year' · participants with glaucoma or ocular hypertension
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Pain (short‐term) Pain index1. Scale from: 0 to 70. · participants with acute or subacute low‐back pain
1 finding from 1 review
Duration of sick‐leave Sick‐leave > 21 days · participants with acute or subacute low‐back pain
It is very uncertain whether back school changes duration of sick‐leave Sick‐leave > 21 days compared with short‐wave diathermy at the lowest intensity (very low certainty).
1 finding from 1 review
Intervention not reported
Clinical outcome: systolic blood pressure (automated sphygmomanometer or electronic pressure monitor) ATCS Plus or IVR versus usual care at median · patients with hypertension
1 finding from 1 review
Intervention not reported
Clinical outcome: diastolic blood pressure (automated sphygmomanometer and electronic cuff) ATCS Plus, unidirectional versus usual care at median · patients with hypertension
1 finding from 1 review
Intervention not reported
Clinical outcome: blood pressure control, 26 weeks Multimodal/complex interventionf versus usual care · patients with hypertension
1 finding from 1 review
Intervention not reported
Clinical outcome: Health statush, depressioni, 6 weeks ATCS Plus versus enhanced usual care (plus information) · patients with hypertension
1 finding from 1 review
Intervention not reported
Behavioural outcome: medication use Multimodal/complexk, ATCS Plus versus usual care or enhanced usual care (plus information) · patients with hypertension
1 finding from 1 review
Intervention not reported
Behavioural outcome: physical activity levels, 12 weeks IVR versus enhanced usual care · patients with hypertension
1 finding from 1 review
Intervention not reported
Adverse outcome: unintended adverse events attributable to the intervention Multimodal/complex intervention, ATCS Plus, IVR, unidirectional ATCS versus various controls · patients with hypertension
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
HRQOL ‐ not measured · Participants with rosacea
The review found no eligible studies for this question.
1 finding from 1 review
Participant‐assessed improvement in rosacea severity · Participants with rosacea
1 finding from 1 review