Kline 2020.
Study characteristics | ||
Methods |
Study design: randomised controlled trial Study grouping: parallel group |
|
Participants |
Baseline characteristics Dog
Coloring
Control (no intervention)
Overall
Included criteria: emergency care providers, including nurses, residents, and physicians on duty in the ED of Eskenazi hospital Excluded criteria: provider statement of dislike, allergy, fear or other reason to not interact with a therapy dog, and prior enrolment Pretreatment: no significant differences in age and gender between the two experimental groups and the control group. Authors did not report any other results. Compliance rate: 127 eligible and 122 participated in at least 50% of the intervention thus > 96% Response rate: NR Type of healthcare worker: nurse, physician resident |
|
Interventions |
Intervention characteristics Dog
Colouring
Control (no intervention)
|
|
Outcomes |
Perceived Stress Scale (PSS)
Stress (VAS)
|
|
Identification |
Sponsorship source: NR Country: USA Setting: Hospital Comments: NR Authors name: Jeffrey A Kline Institution: Indiana University School of Medicine, Indianapolis Email: jefkline@iupui.edu Address: Indiana University School of Medicine, Indianapolis Time period: 2018 |
|
Notes | Author J Kline kindly provided the mean and SD of the primary outcome for the intervention groups. Modified PSS included in analysis 2.1. Intervention groups combined to create a single pair‐wise comparison |
|
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Quote: "were randomized by preprinted random sequence to receive either exposure to a therapy dog or to coloring a mandala." |
Allocation concealment (selection bias) | Unclear risk | Insufficient information to understand whether intervention allocations could have been foreseen in advance of, during, enrolment. |
Blinding of participants and personnel (performance bias) All outcomes | High risk | Participants were not blinded. |
Blinding of outcome assessment (detection bias) All outcomes | High risk | Participants were not blinded whereas outcomes are self‐reported. |
Incomplete outcome data (attrition bias) All outcomes | Low risk | No loss to follow‐up |
Selective reporting (reporting bias) | Low risk | Trial registration NCT03628820. No selective outcome reporting. |
Other bias | Unclear risk | Response rate not reported. |