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临床试验/NCT04215029
NCT04215029进行中(未招募)不适用

Reducing Prostate Cancer Disparities Among African Americans

M.D. Anderson Cancer Center1 个研究点 分布在 1 个国家目标入组 6 人开始时间: 2019年8月27日最近更新:
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
6
试验地点
1
主要终点
Implementing a lifestyle intervention and active surveillance on couple-based behavioral intervention developed for African American (AA) or Hispanic men

研究概览

简要总结

This trial studies how well a lifestyle intervention works in reducing prostate cancer disparities among African American prostate cancer patients and their spouses or romantic partners. A lifestyle intervention may help researchers learn if social support can help African American prostate cancer patients and their partners improve their quality of life, support from their partner, physical activity, diet, and inflammation.

详细描述

PRIMARY OBJECTIVE:

I. To expand an existing couple-based behavioral intervention developed for African American (AA) or Hispanic men on active surveillance (Watchful Living; protocol #: 2017-0556) to AA prostate cancer (PCa) survivors who underwent active treatments to examine its feasibility of recruiting AA PCa survivor-partner dyads (N = 40 dyads) and implementing a lifestyle intervention.

SECONDARY OBJECTIVES:

I. Evaluate a preliminary efficacy of the intervention in improving quality of life, physical activity, nutrient intake, and inflammation.

II. Explore psychosocial mediators and moderators of the intervention. III. Conduct a process evaluation. IV. Assess healthcare-provider level factors (with N=15 providers) that influence both survivors' and partners' healthy lifestyle behaviors.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
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

入选标准

  • To be eligible, prostate cancer survivors must self-identify as black or African American
  • Prostate cancer survivors must have 0-III stage prostate cancer
  • Prostate cancer survivors must have completed therapy (e.g., surgery, chemotherapy [chemo] and/or radiation)
  • Prostate cancer survivors must enroll with a spouse or a romantic partner
  • Prostate cancer survivors must not meet physical activity recommendation (i.e., 150 minutes of moderate intensity physical activity per week)
  • Prostate cancer survivors must be willing and able to be physically active, as determined by responses to the Physical Activity Readiness Questionnaire (PAR-Q)
  • Prostate cancer survivors must not participate in another physical activity, diet, or lifestyle program
  • Prostate cancer survivors must have a valid home address and telephone number
  • Prostate cancer survivors must be able to access internet over a smartphone or a computer at home or other location (e.g., work, church, library, community center, etc.)
  • To be eligible, spouses or romantic partners must be >=18 years of age
  • Spouses or romantic partners must enroll with a spouse or a romantic partner with prostate cancer
  • Spouses or romantic partners must live together with the survivors
  • Spouses or romantic partners must not have major health problems (e.g., cancer, dementia, stroke, and heart and lung diseases)
  • Spouses or romantic partners must be willing and able to be physically active, as determined by responses to the Physical Activity Readiness Questionnaire (PAR-Q)
  • To be eligible, healthcare providers must be currently providing care with individuals diagnosed with prostate cancer
  • Any professionals such as surgical and medical oncologists, fellows, nurse practitioners, physical assistants, and primary care physicians will be eligible

排除标准

  • Prostate cancer survivors will be excluded if they are not married or partnered
  • Prostate cancer survivors will be excluded if they have an active noncutaneous malignancy at any site
  • Prostate cancer survivors will be excluded if they had a prior history of other cancer or have metastatic cancer
  • Prostate cancer survivors will be excluded if they have planned concomitant immunotherapy, hormonal therapy, chemotherapy, or radiation therapy during the study period
  • Prostate cancer survivors will be excluded if they are on active surveillance
  • Prostate cancer survivors will be excluded if they enrolled in a protocol #: 2017-0556
  • Prostate cancer survivors will be excluded if they are not able to understand and speak English
  • Spouses or romantic partners who are not able to understand and speak English will be excluded
  • Also, spouses or romantic partners who enrolled in a protocol (#2017-0556) will be excluded
  • There are no exclusion criteria for healthcare providers

研究组 & 干预措施

Group I (exercise plan, coaching calls, nutrition counseling)

Experimental

Patients and their partners receive an exercise plan and printed materials that includes instructions for walking or other moderate-intensity activities. Patients and their partners also receive coaching calls discussing physical activity and diet related questions, each lasting 45-60 minutes and occurring every 2 weeks for 6 months. In addition, patients and their partners complete 2 nutrition counseling sessions over 1 hour each at baseline and before month 3 with an MD Anderson registered dietitian.

干预措施: Exercise Intervention (Behavioral)

Group I (exercise plan, coaching calls, nutrition counseling)

Experimental

Patients and their partners receive an exercise plan and printed materials that includes instructions for walking or other moderate-intensity activities. Patients and their partners also receive coaching calls discussing physical activity and diet related questions, each lasting 45-60 minutes and occurring every 2 weeks for 6 months. In addition, patients and their partners complete 2 nutrition counseling sessions over 1 hour each at baseline and before month 3 with an MD Anderson registered dietitian.

干预措施: Informational Intervention (Other)

Group I (exercise plan, coaching calls, nutrition counseling)

Experimental

Patients and their partners receive an exercise plan and printed materials that includes instructions for walking or other moderate-intensity activities. Patients and their partners also receive coaching calls discussing physical activity and diet related questions, each lasting 45-60 minutes and occurring every 2 weeks for 6 months. In addition, patients and their partners complete 2 nutrition counseling sessions over 1 hour each at baseline and before month 3 with an MD Anderson registered dietitian.

干预措施: Nutritional Assessment (Other)

Group I (exercise plan, coaching calls, nutrition counseling)

Experimental

Patients and their partners receive an exercise plan and printed materials that includes instructions for walking or other moderate-intensity activities. Patients and their partners also receive coaching calls discussing physical activity and diet related questions, each lasting 45-60 minutes and occurring every 2 weeks for 6 months. In addition, patients and their partners complete 2 nutrition counseling sessions over 1 hour each at baseline and before month 3 with an MD Anderson registered dietitian.

干预措施: Questionnaire Administration (Other)

Group I (exercise plan, coaching calls, nutrition counseling)

Experimental

Patients and their partners receive an exercise plan and printed materials that includes instructions for walking or other moderate-intensity activities. Patients and their partners also receive coaching calls discussing physical activity and diet related questions, each lasting 45-60 minutes and occurring every 2 weeks for 6 months. In addition, patients and their partners complete 2 nutrition counseling sessions over 1 hour each at baseline and before month 3 with an MD Anderson registered dietitian.

干预措施: Telephone-Based Intervention (Behavioral)

Group II (physical activity/healthy eating information)

Active Comparator

Patients and their partners receive information/materials regarding physical activity and healthy eating.

干预措施: Informational Intervention (Other)

Group II (physical activity/healthy eating information)

Active Comparator

Patients and their partners receive information/materials regarding physical activity and healthy eating.

干预措施: Questionnaire Administration (Other)

Provider Interviews (interviews)

Experimental

Healthcare providers participate in an interview regarding their opinions on family-focused care and its ability to improve health behaviors.

干预措施: Interview (Other)

结局指标

主要结局

Implementing a lifestyle intervention and active surveillance on couple-based behavioral intervention developed for African American (AA) or Hispanic men

时间窗: up to 6 months

We will calculate rates of recruitment and retention, along with 90% confidence intervals (CIs). Participant feedback will be summarized using means and standard deviations (SDs)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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