Improving In-hospital Stroke Service Utilisation in China

NCT03317639 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1634

Last updated 2021-08-19

No results posted yet for this study

Summary

A cluster randomised controlled trial will be conducted, using hospital as randomisation unit. Hospitals in Zhejiang Province, China, will be randomised into two arms (1:1): an intervention arm and a control arm. Hospitals in the intervention arm will receive a multi-components intervention based on the Behaviour Change Wheel model, whereas hospitals in the control arm will receive no intervention and maintain existing care. The randomisation will be conducted after one-year baseline data collection. The following baseline data will be used for randomisation match: hospital classification, beds in stroke centre, thrombolysis patient number, and percentage of patients receiving thrombolysis within 60 minutes of stroke onset. Hospitals with no stroke centre or with \<20 cases received thrombolysis per year will be excluded from the study. The primary outcome will be difference between intervention arm and control arm in the percentage of patients receiving thrombolysis within 60 minutes of stroke onset on the follow-up stage (post-intervention).

Conditions

  • Thrombolytic Therapy
  • Acute Stroke
  • Door to Treatment Time
  • Quality Improvement

Interventions

BEHAVIORAL

Behaviour Change Wheel model guided intervention

Interventions are developed on a psychological model, the Behaviour Change Wheel (BCW) .The fundamental of BCW consists of three essential elements: capability, motivation, and opportunity. Improving individual's capability, providing motivation, and increasing opportunities are goals of behaviour change intervention. To achieve the goals, 9 intervention components have been proposed in the BCW framework, and 6 components will be used in current study.

Sponsors & Collaborators

  • Shaoxing Second Hospital

    collaborator OTHER
  • Haining People' s Hospital

    collaborator UNKNOWN
  • Haiyan People' s Hospital

    collaborator UNKNOWN
  • Huzhou No.1 People' s Hospital

    collaborator UNKNOWN
  • Jiashan No.1 People' s Hospital

    collaborator UNKNOWN
  • Ningbo Medical Center Lihuili Hospital

    collaborator OTHER_GOV
  • Tongxiang No.1 People' s Hospital

    collaborator UNKNOWN
  • First Affiliated Hospital of Wenzhou Medical University

    collaborator OTHER
  • Yiwu Central Hospital

    collaborator OTHER
  • Yongkang No.1 People' s Hospital

    collaborator UNKNOWN
  • Yuyao People's Hospital

    collaborator OTHER
  • Deqing People' s Hospital

    collaborator UNKNOWN
  • Dongyang People's Hospital

    collaborator OTHER
  • Jinhua People' s Hospital

    collaborator UNKNOWN
  • Lishui People' s Hospital

    collaborator UNKNOWN
  • Lin' an People' s Hospital

    collaborator UNKNOWN
  • Longquan People' s Hospital

    collaborator UNKNOWN
  • Qingtian People' s Hospital

    collaborator UNKNOWN
  • Shaoxing Central Hospital

    collaborator OTHER
  • Wenzhou Central Hospital

    collaborator OTHER
  • Xiangshan No.1 People' s Hospital

    collaborator UNKNOWN
  • The Central Hospital of Lishui City

    collaborator OTHER
  • Second Affiliated Hospital, School of Medicine, Zhejiang University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-01
Primary Completion
2019-12-31
Completion
2020-06-30

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03317639 on ClinicalTrials.gov