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. 2023 May 12;2023(5):CD002892. doi: 10.1002/14651858.CD002892.pub6

Kline 2020.

Study characteristics
Methods Study design: randomised controlled trial
Study grouping: parallel group
Participants Baseline characteristics
Dog
  • Age (mean ± SD): 31 ± 7.1

  • Sex (N (% female)): 20(50)

  • Sample size: 43

  • Years of experience (mean ± SD): NR


Coloring
  • Age (mean ± SD): 32 ± 7.3

  • Sex (N (% female)): 20(50)

  • Sample size: 39

  • Years of experience (mean ± SD): NR


Control (no intervention)
  • Age (mean ± SD): 33 ± 7.2

  • Sex (N (% female)): 18(49)

  • Sample size: 40

  • Years of experience (mean ± SD): NR


Overall
  • Age (mean ± SD): NR

  • Sex (N (% female)): NR

  • Sample size: 122

  • Years of experience (mean ± SD): NR


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
  • Type of the intervention: Intervention type 2 ‐ to focus one’s attention away from the experience of stress

  • Description of the intervention: Being in a room with a dog, participants were allowed to touch the dog

  • The number of sessions: 1

  • Duration of each session on average: 5 minutes

  • Duration of the entire intervention: beginning of the shift until the end of the shift

  • Duration of the entire intervention short vs long: short

  • Intervention deliverer: NR

  • Intervention form: individual


Colouring
  • Type of the intervention: Intervention type 2 ‐ to focus one’s attention away from the experience of stress

  • Description of the intervention: Colouring mandalas in a room

  • The number of sessions: 1

  • Duration of each session on average: 5 minutes

  • Duration of the entire intervention: beginning of the shift until the end of the shift

  • Duration of the entire intervention short vs long: short

  • Intervention deliverer: NR

  • Intervention form: individual


Control (no intervention)
  • Type of the intervention: NA

  • Description of the intervention: NA

  • The number of sessions: NA

  • Duration of each session on average: NA

  • Duration of the entire intervention: NA

  • Duration of the entire intervention short vs long: NA

  • Intervention deliverer: NA

  • Intervention form:

Outcomes Perceived Stress Scale (PSS)
  • Outcome type: ContinuousOutcome


Stress (VAS)
  • Outcome type: ContinuousOutcome

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.