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Clinical Trials/NCT04215029
NCT04215029
Active, Not Recruiting
N/A

Reducing Prostate Cancer Disparities Among African Americans

M.D. Anderson Cancer Center1 site in 1 country6 target enrollmentAugust 27, 2019

Overview

Phase
N/A
Intervention
Exercise Intervention
Conditions
Not specified
Sponsor
M.D. Anderson Cancer Center
Enrollment
6
Locations
1
Primary Endpoint
Implementing a lifestyle intervention and active surveillance on couple-based behavioral intervention developed for African American (AA) or Hispanic men
Status
Active, Not Recruiting
Last Updated
17 days ago

Overview

Brief Summary

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.

Detailed Description

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. OUTLINE: Patients and their partners are randomized to 1 of 2 groups. GROUP I: 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. GROUP II: Patients and their partners receive information/materials regarding physical activity and healthy eating. PROVIDER INTERVIEWS: Healthcare providers participate in an interview regarding their opinions on family-focused care and its ability to improve health behaviors.

Registry
clinicaltrials.gov
Start Date
August 27, 2019
End Date
July 31, 2026
Last Updated
17 days ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 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

Exclusion Criteria

  • 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

Arms & Interventions

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

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.

Intervention: Exercise Intervention

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

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.

Intervention: Informational Intervention

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

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.

Intervention: Nutritional Assessment

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

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.

Intervention: Questionnaire Administration

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

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.

Intervention: Telephone-Based Intervention

Group II (physical activity/healthy eating information)

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

Intervention: Informational Intervention

Group II (physical activity/healthy eating information)

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

Intervention: Questionnaire Administration

Provider Interviews (interviews)

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

Intervention: Interview

Outcomes

Primary Outcomes

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

Time Frame: 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)

Study Sites (1)

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