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临床试验/NCT02018471
NCT02018471已完成不适用

Management of Anxiety Related to Diagnostic Screenings: an Exploratory Pilot Study

Istituto Oncologico Veneto IRCCS0 个研究点目标入组 43 人开始时间: 2012年4月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
43
主要终点
Proportion of patients considered drop-outs

研究概览

简要总结

Diagnostic tests have a deep emotional impact on oncology patients. Anxiety and worries can lead people to avoid screening tests, with high risks for health. A single arm, pilot study was organized to evaluate the feasibility and efficacy of psychological counselling for cancer patients who demonstrated anxiety for diagnostic tests. The hypothesis was that taking part in Psychoeducative Training could offer a new modality to reduce anxiety, before and during tests, and also the possibility to reinforce coping strategies.

详细描述

The Psychoeducative Training was organized in 6 weekly meetings lasting two hours. Each group was composed of 6 participants. The Training follows the cognitive-behavioural model. In the first part of every meeting, theoretical aspects about stress and anxiety were explained, while in the second part some relaxation techniques were taught. During relaxation, we used a selected music that was also going to be used during the diagnostic tests. Since the first meeting, patients experienced these relaxing techniques in order to learn them. In order to support the adaptability, at the end of every meeting the participants received some homework. They had to take notes on how many times they repeated the relaxation exercises and on the anxiety level before and after the training.

For the study, 43 people were recruited. Anxiety was measured with Beck Anxiety Inventory (BAI); it values the seriousness of the physiological behaviour connected with anxiety. This test an "anxiety gauge", which allows us to obtain numerical data on emotional changes. The test is composed of 4 interpretative levels: serious, moderate, small and minimal anxiety.

The coping style was measured with Coping Orientation to Problems Experienced-New Italian Version (COPE-NIV); this test evaluates the way in which people resolve and face traumatic or usual stressful situations.

The research project was approved by the Ethics Committee of Veneto Institute of Oncology.

Every patient signed a written informed consent to process the data for research purposes and to publish it.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
25 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • age: 25 to 65 years cancer patients who must undergo diagnostic tests: TAC, PET, fMRI, Mammography, Endoscopy and Colonoscopy.
  • an anxiety level greater than 5 (in a scale from 0=very calm to 10=very anxious; using a self-reporting instrument created ad hoc)
  • signed informed consent

排除标准

  • healthy people

结局指标

主要结局

Proportion of patients considered drop-outs

时间窗: 6 weeks after recruitment (end of treatment)

The proportion of patients considered drop-outs. A patient is considered a drop-out if he/she does not attend at least 2 out of 6 programmed meetings. This is a feasibility outcome

次要结局

  • median BAI score after intervention(6 weeks after recruitment (end of treatment))
  • median COPE score - Social support score after intervention(6 weeks after recruitment (end of treatment))
  • median COPE score - Positive attitude score after intervention(6 weeks after recruitment (end of treatment))
  • median COPE score - Problem acceptance score after intervention(6 weeks after recruitment (end of treatment))
  • recruitment time (process)(6 weeks after recruitment (end of treatment))
  • number of questionnaires correctly filled out (process)(6 weeks after recruitment (end of treatment))
  • phone lines overloaded or waiting room overcrowded by study participants (management)(6 weeks after recruitment (end of treatment))
  • median COPE score - Avoidance strategies score after intervention(6 weeks after recruitment (end of treatment))
  • mean number of recruited patients per week (process)(6 weeks after recruitment (end of treatment))
  • refusal rate among eligible patients (process)(6 weeks after recruitment (end of treatment))
  • rate of patients who obviously meet and do not meet the eligibility requirements (process)(6 weeks after recruitment (end of treatment))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Malihe Shams

Psychologist

Istituto Oncologico Veneto IRCCS

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