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临床试验/NCT05679518
NCT05679518招募中不适用

Managing Fear of Cancer Progression Metacognition-based Vs Supportive-expressive Based Approaches: A Randomized Controlled Trial

The University of Hong Kong4 个研究点 分布在 1 个国家目标入组 284 人开始时间: 2023年12月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
284
试验地点
4
主要终点
Fear of Progression

研究概览

简要总结

The present study aims to conduct a randomized controlled trial to assess the effect of CALM intervention and ConquerFear intervention on fear of cancer progression among Chinese patients diagnosed with advanced cancer.

详细描述

A randomized controlled trial will be conducted to assess the effect of CALM intervention and ConquerFear intervention on fear of cancer progression among Chinese patients diagnosed with advanced cancer.

The aims are to test:

  1. the direct effect of CALM intervention or ConquerFear intervention on fear of cancer progression, and
  2. the indirect effect of ConquerFear intervention on fear of cancer progression through its effect on maladaptive metacognition.

Primary hypothesis:

  1. Patients receiving CALM intervention or ConquerFear intervention, compared to those receiving a basic cancer care intervention will show a reduction in fear of cancer progression.
  2. Both CALM intervention and ConquerFear intervention will be equally effective in reducing fear of cancer progression.
  3. Given ConquerFear intervention aims to modify unhelpful metacognitive beliefs, there will be an indirect effect of ConquerFear intervention on fear of cancer progression through its effect on maladaptive metacognition.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

盲法说明

The investigator, care provider, and outcomes assessor are masked in terms of not knowing to which condition the participants will be randomized until after the completion of the baseline assessment. The outcomes assessor will break the envelope for the next eligible participant indicating if that participant is to be allocated to ConquerFear or CALM or control arms.

The participants are masked in terms of not knowing that the interventions (i.e. Conquer fear and CALM) are hypothesized to yield larger effects than the other (i.e. control).

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

  • •Cantonese- or Mandarin-speaking Chinese patients recently diagnosed with advanced or metastatic (i.e. stage III or IV) cancer
  • •are the age of 18 years or above

排除标准

  • •Patients with major communication difficulties
  • •are being unwilling or unable to commit 6 psychotherapy sessions

研究组 & 干预措施

ConquerFear intervention

Experimental

Participants in the ConquerFear intervention group will receive a manualized intervention, consisting of 6 therapist-led individual sessions.

干预措施: ConquerFear intervention (Behavioral)

CALM intervention

Experimental

Participants in the CALM intervention group will receive a semi-structured, manualized, individual psychotherapy intervention consisting of 3-6 individual therapy sessions.

干预措施: CALM intervention (Behavioral)

Basic Cancer Care

Active Comparator

Basic Cancer Care serves as an active comparator and is not developed specifically to target fear of cancer recurrence through modifying participants' cognitive beliefs. Participants in this arm will receive 6 individual sessions including 2 relaxation training sessions, 2 dietetic consultation sessions, and 2 exercise sessions, which will be led by a trained therapist, a registered dietitian, and an exercise physiologist, respectively.

干预措施: Basic Cancer Care (Behavioral)

结局指标

主要结局

Fear of Progression

时间窗: Baseline, the immediate post-intervention, 3-months post-intervention and 6-months post-intervention

The 12-item short version of the Fear of Progression Questionnaire (FoP-Q-SF) will be used to assess the change in total score of fear of caner progression. Each item of the FoP-Q-SF is rated on 5-point Likert scales anchored at 1 (Never) to 5 (very often). Higher scores indicate higher levels of fear of cancer progression. Total scores range from 12 to 60. A cutoff of 24-33 was used to suggest subthreshold level of fear of progression and a score of 34 or greater suggest high levels of fear of progression.

次要结局

  • Metacognitions(Baseline, the immediate post-intervention, 3-months post-intervention and 6-months post-intervention)
  • Depression(Baseline, the immediate post-intervention, 3-months post-intervention and 6-months post-intervention)
  • Death anxiety(Baseline, the immediate post-intervention, 3-months post-intervention and 6-months post-intervention)

研究者

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

Wendy Wing Tak Lam

Associate Professor

The University of Hong Kong

研究点 (4)

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