Tucker 1989.
| Study characteristics | ||
| Methods |
Study design
Duration of study
Duration of follow‐up
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| Participants |
General information
Baseline characteristics
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| Interventions |
Intervention type
Intervention group 1
Intervention group 2
Intervention group 3
Control group
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| Outcomes | Potassium Daily fluid gain Social support scale Compliance |
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| Notes |
Conflict of interest
Funding source
Other information
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| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Random sequence generation (selection bias) | Low risk | Randomised block procedure |
| Allocation concealment (selection bias) | Unclear risk | Insufficient information to permit judgement |
| Blinding of participants and personnel (performance bias) All outcomes | High risk | Participants were not blinded. No mention of whether staff blinded Nursing staff giving intervention could not have been blinded |
| Blinding of outcome assessment (detection bias) Subjective outcomes | High risk | Self reported fluid intake |
| Blinding of outcome assessment (detection bias) Objective outcomes | Low risk | Medical record data for IDWG |
| Incomplete outcome data (attrition bias) All outcomes | Unclear risk | No mention of loss to follow‐up |
| Selective reporting (reporting bias) | Unclear risk | Insufficient information to permit judgement |
| Other bias | Unclear risk | Monetary gifts, short follow‐up period |