跳至主要内容
临床试验/ISRCTN18000119
ISRCTN18000119进行中(未招募)未知

Vertebral fracture clinical decision tool for older women with back pain (Vfrac) - a feasibility study

niversity of Bristol0 个研究点目标入组 32 人开始时间: 2022年3月1日最近更新:
适应症

试验速览

阶段
未知
状态
进行中(未招募)
发起方
入组人数
32

研究概览

简要总结

2024 Protocol article in https://doi.org/10.1007/s11657-023-01364-1 (added 07/02/2024)

研究设计

研究类型
Interventional

入排标准

性别
Female

入选标准

  • WP1: Recruitment of general practices only - no individual patients
  • 1. General practices willing to take part in research within the Bristol area
  • WP2: nested qualitative assessment of acceptability - recruitment of patients and healthcare professionals
  • Inclusion criteria for patients:
  • 1. Female aged >65 years
  • 2. Had Vfrac used during a consultation for back pain
  • 3. Patient is willing and able to give informed consent for participation in this nested evaluation
  • Inclusion criteria for healthcare professionals:
  • 1. Used Vfrac during a consultation for back pain OR were involved in the implementation of Vfrac within IT systems or clinical pathways within one of the three intervention practices
  • 2. Healthcare professional is willing and able to give informed consent for participation in this nested evaluation

排除标准

  • WP1: Recruitment of general practices only - no individual patients
  • Does not meet the inclusion criteria
  • WP2: nested qualitative assessment of acceptability - recruitment of patients and healthcare professionals
  • Exclusion criteria for patients:
  • 1. Has not had Vfrac used during a consultation for back pain
  • 2. Patients who do not have the capacity to provide informed consent. Capacity to consent will be assessed by the researcher, in consultation with clinical members of the study team (EC). This is in accordance with the Mental Capacity Act 2005 (https://www.hra.nhs.uk/planning-and-improving-research/policies-standards-legislation/mental-capacity-act/).
  • 3. Participants who are unwilling to provide informed consent
  • Exclusion criteria for healthcare professionals:
  • 1. Participants who are unwilling to provide informed consent

研究者

发起方
niversity of Bristol

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