跳至主要内容
临床试验/NCT02862002
NCT02862002Unknown不适用

Measuring the Effects of Therapeutic Education Program "Caratif" Patient Under Strong Opioids Versus Standard Taking Charge of Patient Pain Receiving Opioid Therapy in Medical Oncology.

Assistance Publique Hopitaux De Marseille2 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2013年8月最近更新:
适应症

试验速览

阶段
不适用
入组人数
200
试验地点
2
主要终点
Pain assessment

研究概览

简要总结

A first empirical evidence on the difficulties of observance of morphine in cancer patients invited a multidisciplinary team to initiate an innovative quality approach. It shows the lack of transcript of a comprehensive care causing a problem for monitoring actions undertaken for the relief of pain. In addition, two exploratory studies targeting the expectations and needs of the Patient Therapeutic Education (E.T.P) receiving strong opioids.

The E.T.P, public health priority, provides a framework for action and improving care. In oncology, the involvement of the patient in pain relief and management of opioids represents an axis of intervention more appropriate. Yet, it is not found in literature. In our department, we conduct an experimental therapeutic education program type "caratif" and a nurse consultation FTE receiving opioids on the model of nursing "care" of J. Watson (humanist emphasis promoting interpersonal teaching-learning mobilizing the patient experience). The ETP folder and its tools have been continuously validated with patients. The heart of the educational process is in the patient's complex path neat oncology and relies on interaction and creativity between patient and caregivers.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Cancer patients receiving opioids
  • Suffering from pain caused by their disease or treatment with chemotherapy and / or radiotherapy and / or surgery
  • Supported within the oncology or palliative care
  • Receiving at least 3 courses of chemotherapy
  • Having read, understood and signed the informed consent
  • Subject beneficiary of a social security scheme or an equivalent -

排除标准

  • adults subject to a legal protection measure or unable to consent
  • Non-beneficiaries of a social security scheme,
  • persons deprived of liberty by a judicial or administrative decision,
  • patients with neurological or psychiatric disorders

结局指标

主要结局

Pain assessment

时间窗: 21 days

Using a digital scale

次要结局

  • Treatment adherence morphine(21 days)
  • Anxiety(21 days)
  • Strategies Adjustment disease(21 days)
  • Depression(21 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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