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临床试验/ACTRN12623001020673
ACTRN12623001020673招募中Unknown

A multi-centre, single-arm, phase II feasibility study of the feasibility and acceptability of meditation on symptoms of psycho-existential distress and anxiety in people with advanced cancer who are receiving palliative care.

niversity of Technology Sydney0 个研究点目标入组 42 人开始时间: 2023年9月20日最近更新:
适应症

试验速览

阶段
Unknown
状态
招募中
入组人数
42

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Non-randomised trial
主要目的
Treatment
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • 1. Aged greater than or equal to 18 years
  • 2.Clinician responds ‘no’ to the surprise question ‘Would you be surprised if the patient were to die within the next 12 months
  • 3.The patient has a life expectancy of at least 3 months in the opinion of the treating clinician
  • 4.Screen positive for psycho-existential distress (PESAS subscale score greater than or equal to 4)
  • 5.Sufficient English to participate in interviews, study interventions and complete questionnaires
  • 6.Able to maintain attention for 20 minutes
  • 7.Willing to provide informed written, digital or audio-recorded consent.

排除标准

  • 1.Cognitive impairment to the extent that it impairs patients from completing questionnaires and interviews describing their experiences
  • 2.Pre-existing severe psychotic illness (e.g., poorly controlled psychosis, schizo-affective disorder, manic bipolar disorder)
  • 3.New onset or re-occurrence of post-traumatic stress disorder within the last month
  • 4.Delirium (clinician assessed)
  • 5.Terminal phase (Palliative care Outcomes Collaboration (PCOC) Phase 4.

研究者

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