跳至主要内容
临床试验/NCT06485310
NCT06485310撤回不适用

Interest of a TEteleconsultation of a Psychological Support Nurse on Psychological Distress in Patients With a Primary Malignancy of the Central Nervous System Between the Announcement of the Diagnosis and the First Treatment

Centre Hospitalier Universitaire de la Réunion1 个研究点 分布在 1 个国家目标入组 58 人开始时间: 2026年3月31日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
发起方
入组人数
58
试验地点
1
主要终点
Distress thermometer

研究概览

简要总结

The goal of this clinal trial is to compare the effectiveness of nurse-led teleconsultation with usual care (intervention group) on psychological distress in patients with primary malignant tumors of the central nervous system between diagnosis and first anti-cancer treatment, versus usual care alone (control group).

Participants will be randomized into two groups :

  • group A) intervention: usual care + nurse teleconsultation for psychological support
  • group B) control: usual care alone

Enrolment = Day0 (D0)

Participants will :

  • groups A and B: D0: complete 4 questionnaires (Quality of Life, Screening for Distress, Screening for Anxiety and Depression, Social Support Questionnaire)
  • Group A : D0+2/4 das : nursing teleconsultation for psychological support
  • Groups A and B: D0+10days : telephone call to complete the same 4 questionnaires as at inclusion
  • Group A : D0+15days: semi-directive interview, at home, for voluntary patients.

详细描述

The expected benefits are as follows:

For the patient :

  • Reduction in pre-treatment psychological distress
  • Reduced pre-treatment anxiety and depression
  • Better understanding of disease and treatments
  • Better adherence to the care proposed in the treatment pathway
  • Reduced stress during first hospital treatment

For healthcare professionals :

  • Early detection of psychological distress
  • Early detection of unmet needs and appropriate individualized responses
  • Establishment of a climate of trust between patient and caregiver
  • Improved professional practices

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
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
否

入选标准

  • •aged 18 and over
  • •being treated for a primary malignant tumor of the central nervous system (positive biopsy)
  • •with a Mini-Mental State score greater than 24
  • •not receiving first-line treatment (chemotherapy, targeted radiotherapy, surgery)
  • •with a distress score above 3 on the Psychological Distress Thermometer
  • •have access to computer equipment equipped with a microphone and webcam (smartphone, computer)
  • •able to read, write and speak French
  • •have given free and informed consent
  • •being affiliated to a social security scheme

排除标准

  • •with a history of psychiatric illness
  • •with recurrent cancer of the cerebral nervous system
  • •having begun first-line treatment (drug therapy, curative surgery, radiotherapy or palliative care)
  • •under guardianship, curatorship or deprived of liberty

研究组 & 干预措施

TELECONSULTATION

Experimental

Teleconsultation with a nurse for psychological support, after the diagnosis has been announced, before hospitalization for the first treatment (chemotherapy, surgery, radiotherapy) in addition to the standard practice.

干预措施: Teleconsultation for psychological support (Other)

NO TELECONSULTATION

No Intervention

The control group will be cared for according to standard practice (without teleconsultation)

结局指标

主要结局

Distress thermometer

时间窗: 10 days

Comparison of the change in psychological distress score, measured using the psychological distress screening tool (from National Comprehensive Cancer Network) between the 2 groups between inclusion (T0) and before the first anti-cancer therapy (T1).

次要结局

未报告次要终点

研究者

发起方
Centre Hospitalier Universitaire de la Réunion
申办方类型
Other
责任方
Sponsor

研究点 (1)

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