Trial name | Population | Host trial intervention and comparison | Design of the host trial | Design of SWAT |
---|---|---|---|---|
GHT2000 [21] | Inactive 18–74-year-olds with hypertension, suspected hypertension, pre-hypertension or high-normal blood pressure | Interventions: (i) GP gym-based referral plus web tool, (ii) sport referral (iii) sport referral plus web tool Comparator: GP gym-based referral | Individually randomised four-arm group trial | Two-arm trial, individually randomised |
PSM COPD [22] | COPD patients aged 18 years or older with mild dyspnoea | Intervention: a telephone-based self-management intervention Comparator: usual care | Individually randomised two-arm group trial | Two-arm trial, clustered by general practice |
HI-Light [23] | Patients aged 5 years and over with vitiligo | Interventions: (i) Handheld narrowband UVB (NB-UVB) and (ii) a combination of potent topical corticosteroid and NB-UVB, compared with potent topical corticosteroid | Individually randomised three-arm, placebo-controlled | Two-arm trial, individually randomised |
seAFOod [24] | Patients aged 55–73 years identified during screening colonoscopy as being at ‘high risk’ for subsequent surveillance colonoscopy | Interventions: (i) 2 g eicosapentaenoic acid per day and (ii) 300 mg aspirin per day Comparator: placebo | Individually randomised 2 by 2 factorial trial | Two-arm trial, cluster randomised ( Endoscopy Unit taking part in the UK NHS Bowel Cancer Screening Programme) |
STOP ACEi [20] | Patients with advanced progressive CKD receiving angiotensin-converting enzyme inhibitor or angiotensin receptor blockers (or both) | Intervention: Discontinue Angiotensin Converting enzyme inhibitor (ACEi)/Angiotensin Receptor Blocker (ARB) or combination of both Comparator: Continue ACEi, ARB or combination of both | Individually randomised two-arm group trial | Two-arm trial, individually randomised |