跳至主要内容
临床试验/NCT04727710
NCT04727710终止不适用

Testing the Effect of Mindfulness for Prostatectomy Outcomes (TEMPO)

University of Michigan Rogel Cancer Center1 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2020年8月26日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
1
试验地点
1
主要终点
Change in level of distress assessed using the Patient-Reported Outcomes Measurement Information System (PROMIS) Short Form (SF) Anxiety

研究概览

简要总结

This research project has 2 parts: The first part of the research is to develop a couples-based group mindfulness intervention for men undergoing prostatectomy, with input from patients and their partners. The second part is the trial registered here, which will pilot the researchers' mindfulness intervention, developed in part 1, and observe any reduction of distress for men undergoing prostatectomy and their partners.

详细描述

In part 1 of this research, researchers developed a couples-based group mindfulness intervention for men undergoing prostatectomy, with input from patients and their partners. Three patients who had previously undergone prostatectomy, and had expressed interest in participating in future research endeavors, and their partners were recruited to inform the design of the intervention. This group of six stakeholders identified the types of distress experienced by newly diagnosed prostate cancer patients and their partners, as well as their favored intervention approaches. These stakeholders do participate in the intervention or control groups in part 2 of this study.

Researchers used thematic analysis to assess the type of distress identified by stakeholders as well as approaches favored by them. They mapped these themes on the available mindfulness approaches, identified in their review, to develop an intervention that best captures the concerns of prostate cancer survivors and partners.

Part 2 is the pilot study. Researchers will enroll 20 more couples (men who are planning to undergo radical prostatectomy and their partners) to participate in a pilot study of the intervention. The pilot study will have 2 cohorts (groups). Half of the couples will be randomly assigned to the mindfulness intervention (intervention group) and the other half will receive the usual care (control group). All participants in the intervention and control groups in part 2 of the study will be analyzed to determine the effects and feasibility of the intervention.

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 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Part 2--Pilot study:
  • •Inclusion Criteria
  • •Patients aged 35 - 90 who are planning to undergo radical prostatectomy at University of Michigan Hospital
  • •Partners of these men, aged 18 and older

排除标准

  • •Participants cannot be less than 18 years of age

研究组 & 干预措施

Part 2: Usual care

Active Comparator

Usual care

干预措施: Usual Care (Behavioral)

Part 2: Couples-based mindfulness intervention

Experimental

Mindfulness-based intervention + Usual care

干预措施: Mindfulness-based Intervention (Behavioral)

Part 2: Couples-based mindfulness intervention

Experimental

Mindfulness-based intervention + Usual care

干预措施: Usual Care (Behavioral)

结局指标

主要结局

Change in level of distress assessed using the Patient-Reported Outcomes Measurement Information System (PROMIS) Short Form (SF) Anxiety

时间窗: Change from baseline at 3 and 6 months post-prostatectomy

This survey is administered as part of the patient's standard clinical care at University of Michigan. PROMIS SF Anxiety is an 8 item scale, each item is scored 1-5 where 1 is never and 5 is always. Higher scores indicate higher levels of anxiety.

Change in level of distress assessed using the PROMIS SF Depression.

时间窗: Change from baseline at 3 and 6 months post-prostatectomy

This survey is administered as part of the patient's standard clinical care at University of Michigan. PROMIS SF Depression is an 8 item scale, each item is scored 1-5 where 1 is never and 5 is always. Higher scores indicate higher levels of depression.

Change in level of distress assessed using the PROMIS SF Positive Affect and Well Being

时间窗: Change from baseline at 3 and 6 months post-prostatectomy

This survey is administered as part of the patient's standard clinical care at University of Michigan. PROMIS SF Positive Affect and Well Being is an 8 item scale, each item is scored 1-5 where 1 is never and 5 is always. Higher scores indicate higher levels of positive affect and well being.

次要结局

  • Change in salivary cortisol level (only patients will complete this, not partners)(Change from baseline at 3 months post-prostatectomy)
  • Change in level of distress assessed using the National Comprehensive Cancer Network (NCCN) Distress Thermometer(Change from baseline to 3 months post-prostatectomy)
  • Change in level of distress assessed using the 5-facet Mindfulness Questionnaire (FFMQ)(Change from baseline at 3 months post-prostatectomy)
  • Change in urinary and sexual function assessed using Michigan Urological Surgery Improvement Collaborative (MUSIC) Expanded Prostate Cancer Index Composite (EPIC-26)(Change from baseline at 3 and 6 months post-prostatectomy)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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