| Recruitment status | Preinitiation |
| Unique ID issued by UMIN | UMIN000041643 |
| Receipt No. | R000045169 |
| Scientific Title | Comparison of learners' performance and subjective workload in rapid cycle deliberate practice and traditional simulation in pediatric anesthesia: a pilot study |
| Date of disclosure of the study information | 2020/10/01 |
| Last modified on | 2022/03/05 (Ver. 2) |
| Basic information | ||
| Public title | Comparison of learners' performance in rapid cycle deliberate practice and traditional simulation in pediatric anesthesia: a pilot study | |
| Acronym | Comparison of learners' performance in rapid cycle deliberate practice and traditional simulation in pediatric anesthesia: a pilot study | |
| Scientific Title | Comparison of learners' performance and subjective workload in rapid cycle deliberate practice and traditional simulation in pediatric anesthesia: a pilot study | |
| Scientific Title:Acronym | Comparison of learners' performance and subjective workload in rapid cycle deliberate practice and traditional simulation in pediatric anesthesia: a pilot study | |
| Region |
|
|
| Condition | ||
| Condition | healthy adults | |
| Classification by specialty |
|
|
| Classification by malignancy | Others | |
| Genomic information | NO | |
| Objectives | |
| Narrative objectives1 | To describe and compare the learners' technical s skills scores and non-technical skills scores in rapid cycle deliberate practice (RCDP) and traditional style simulation |
| Basic objectives2 | Others |
| Basic objectives -Others | To describe and compare the learners' subjective workload in rapid cycle deliberate practice (RCDP) and traditional style simulation |
| Trial characteristics_1 | Confirmatory |
| Trial characteristics_2 | Explanatory |
| Developmental phase | Not applicable |
| Assessment | |
| Primary outcomes | Technical skills assessment score developed by the research team
Anesthesia non-technical skills score NASA LTX All assessment simulation sessions will be video recorded which will be reviewed by two independent raters within 5 months |
| Key secondary outcomes | |
| Base | |
| Study type | Interventional |
| Study design | |
| Basic design | Parallel |
| Randomization | Non-randomized |
| Randomization unit | |
| Blinding | Open -but assessor(s) are blinded |
| Control | Active |
| Stratification | NO |
| Dynamic allocation | NO |
| Institution consideration | Institution is not considered as adjustment factor. |
| Blocking | NO |
| Concealment | Numbered container method |
| Intervention | ||
| No. of arms | 2 | |
| Purpose of intervention | Educational,Counseling,Training | |
| Type of intervention |
|
|
| Interventions/Control_1 | Rapid cycle deliberate practice will be used in a training sessions by a facilitator. Participants will complete 4 pediatric anesthesia simulation scenarios(1 hour for each session) created with a consensus among independent 3 outside board certified anesthesiologists. Pre and post-assessment simulation sessions will be conducted for each scenario in each participant. All of the assessment simulation sessions will be video recorded and will be assessed by independent 2 raters later. | |
| Interventions/Control_2 | Traditional style simulation practice will be used in a training sessions by a facilitator. Participants will complete 4 pediatric anesthesia simulation scenarios(1 hour for each session) created with a consensus among independent 3 outside board certified anesthesiologists. Pre and post-assessment simulation sessions will be conducted for each scenario in each participant. All of the assessment simulation sessions will be video recorded and will be assessed by independent 2 raters later. | |
| Interventions/Control_3 | ||
| Interventions/Control_4 | ||
| Interventions/Control_5 | ||
| Interventions/Control_6 | ||
| Interventions/Control_7 | ||
| Interventions/Control_8 | ||
| Interventions/Control_9 | ||
| Interventions/Control_10 | ||
| Eligibility | ||||
| Age-lower limit |
|
|||
| Age-upper limit |
|
|||
| Gender | Male and Female | |||
| Key inclusion criteria | Pediatric anesthesia fellows and junior anesthesiologists who are younger than post-graduate-year 10 at Aichi Children's Health and Medical Center | |||
| Key exclusion criteria | Subjects who denied the study participation with any reasons | |||
| Target sample size | 10 | |||
| Research contact person | |||||||
| Name of lead principal investigator |
|
||||||
| Organization | Aichi Children's Health and Medical Center | ||||||
| Division name | Anesthesiology | ||||||
| Zip code | 474-8710 | ||||||
| Address | 7-426, Morioka-cho, Obu city, Aichi, Japan | ||||||
| TEL | 0562-43-0500 | ||||||
| daiki_kojima@sk00106.achmc.pref.aichi.jp | |||||||
| Public contact | |||||||
| Name of contact person |
|
||||||
| Organization | Aichi Children's Health and Medical Center | ||||||
| Division name | Anesthesiology | ||||||
| Zip code | 474-8710 | ||||||
| Address | 7-426, Morioka-cho, Obu city, Aichi, Japan | ||||||
| TEL | 0562-43-0500 | ||||||
| Homepage URL | |||||||
| daiki_kojima@sk00106.achmc.pref.aichi.jp | |||||||
| Sponsor | |
| Institute | Aichi Children's Health and Medical Center |
| Institute | |
| Department | |
| Funding Source | |
| Organization | Aichi Children's Health and Medical Center |
| Organization | |
| Division | |
| Category of Funding Organization | Self funding |
| Nationality of Funding Organization | |
| Other related organizations | |
| Co-sponsor | |
| Name of secondary funder(s) | |
| IRB Contact (For public release) | |
| Organization | Aichi Children's Health and Medical Center |
| Address | 7-426, Morioka-cho, Obu city, Aichi, Japan |
| Tel | 0562-43-0500 |
| kenzi_okada@sk00106.achmc.pref.aichi.jp | |
| Secondary IDs | |
| Secondary IDs | NO |
| Study ID_1 | |
| Org. issuing International ID_1 | |
| Study ID_2 | |
| Org. issuing International ID_2 | |
| IND to MHLW | |
| Institutions | |
| Institutions | |
| Other administrative information | |||||||
| Date of disclosure of the study information |
|
||||||
| Related information | |
| URL releasing protocol | |
| Publication of results | Unpublished |
| Result | ||
| URL related to results and publications | ||
| Number of participants that the trial has enrolled | ||
| Results | ||
| Results date posted | ||
| Results Delayed |
|
|
| Results Delay Reason | The participant's inclusion has not been initiated due to COVID surge in Japan | |
| Date of the first journal publication of results | ||
| Baseline Characteristics | ||
| Participant flow | ||
| Adverse events | ||
| Outcome measures | ||
| Plan to share IPD | ||
| IPD sharing Plan description | ||
| Progress | |||||||
| Recruitment status | Preinitiation | ||||||
| Date of protocol fixation |
|
||||||
| Date of IRB | |||||||
| Anticipated trial start date |
|
||||||
| Last follow-up date |
|
||||||
| Date of closure to data entry | |||||||
| Date trial data considered complete | |||||||
| Date analysis concluded | |||||||
| Other | |
| Other related information | |
| Management information | |||||||
| Registered date |
|
||||||
| Last modified on |
|
||||||
| Link to view the page | |
| URL(English) | https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000045169 |