Data Collection

Cross-source consensus on Data Collection from 1 sources and 5 claims.

1 sources · 5 claims

Uses

A data collection procedure confers participant status when it informs a study outcome and involves researcher interaction with providers or collection of identifiable private provider information. — Practical guide for determining whether healthcare providers are research participants in cluster randomised trials
Direct observation of identifiable provider behaviour in clinical settings can confer participant status when it informs a study outcome. — Practical guide for determining whether healthcare providers are research participants in cluster randomised trials
Patient medical records can contain identifiable information about provider decisions that makes providers participants when used for a study outcome. — Practical guide for determining whether healthcare providers are research participants in cluster randomised trials
Treatment fidelity data do not necessarily make healthcare providers research participants. — Practical guide for determining whether healthcare providers are research participants in cluster randomised trials
Provider behaviour data used only to monitor whether an intervention was delivered as planned are process or fidelity data rather than outcome data. — Practical guide for determining whether healthcare providers are research participants in cluster randomised trials