- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01900561
Optimizing Veteran-Centered Prostate Cancer Survivorship Care
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Michigan
-
Ann Arbor, Michigan, United States, 48105
- VA Ann Arbor Healthcare System, Ann Arbor, MI
-
-
Missouri
-
Saint Louis, Missouri, United States, 63106
- St. Louis VA Medical Center John Cochran Division, St. Louis, MO
-
-
Ohio
-
Cleveland, Ohio, United States, 44106
- Louis Stokes VA Medical Center, Cleveland, OH
-
-
Pennsylvania
-
Pittsburgh, Pennsylvania, United States, 15240
- VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Veteran patient at one of the four study sites (Ann Arbor VA, Cleveland VA, Pittsburgh VA, St. Louis VA)
- History of treatment for prostate cancer treated by surgery, radiation or androgen deprivation therapy between 1-10 years prior to identification
Exclusion Criteria:
- No phone number on file
- Not able to converse on the telephone in English
- Treated for metastatic disease or non-prostate cancer
- Dementia or other significant mental impairment
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: IVR Intervention
The intervention will consist of two components, both with content design based on established theories for self-management support: 1) automated telephone monitoring of PC survivor symptoms and goals for symptom reduction, based on a patient empowerment approach, and 2) personally tailored newsletters that incorporate elements of CBT to improve survivors' identification with the material, confidence/self-efficacy in symptom management, and to reduce common cognitive distortions related to successful implementation of behavior change.
Intervention-group participants will receive four automated assessment and self-management support calls over a 3-month period (at baseline, 1-month, 2-month, 3-months).
Information collected during automated phone assessments will be used to construct tailored newsletters, which will be sent following each automated call.
|
The Interactive Voice Response (IVR) system will provide automated telephone monitoring of PC survivor symptoms and goals for symptom reduction, based on a patient empowerment approach.
Personally tailored newsletters will incorporate elements of CBT to improve survivors' identification with the material, confidence/self-efficacy in symptom management, and to reduce common cognitive distortions related to successful implementation of behavior change.
Information collected during automated phone assessments will be used to construct tailored newsletters, which will be sent following each automated call.
|
|
No Intervention: Enhanced Usual Care
Because of the strong evidence documenting symptom burden in PC survivors, the investigators believe that providing control subjects with some information about symptom self-management is warranted.
The investigators further believe, based on the investigators' prior experience conducting RCTs, that offering some type of educational material for Veterans randomized to the control arm will increase their willingness to enroll in the study (as opposed to a pure usual care arm where they would not receive any such materials).
Therefore, survivors randomized to the control condition will receive written material at the time of enrollment designed to educate them about PC symptoms and symptom management.
Material will be approximately six pages in length, also written at or below an 8th grade reading level, and will include a summary of common symptoms experienced by prostate cancer survivors.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Expanded Prostate Cancer Index (EPIC) - Urinary Health, Irritative
Time Frame: Baseline
|
The EPIC is a 26-item measure that assesses symptom burden in four domains: urinary symptoms, bowel symptoms, sexual symptoms and vitality.
Each domain has a subscale related to function and bother which together contribute to disease specific quality of life.
Each domain has a range of possible scores from 0 to 100, with lower scores indicating worse symptom burden.
Lower EPIC scores for any one domain are associated with lower function in that domain and lower QOL.
Thus higher symptom burden, which reflects both function and bother scores, translate into lower EPIC scores.
|
Baseline
|
|
The Expanded Prostate Cancer Index (EPIC) - Urinary Health, Obstructive
Time Frame: Baseline
|
The EPIC is a 26-item measure that assesses symptom burden in four domains: urinary symptoms, bowel symptoms, sexual symptoms and vitality.
Each domain has a subscale related to function and bother which together contribute to disease specific quality of life.
Each domain has a range of possible scores from 0 to 100, with lower scores indicating worse symptom burden.
Lower EPIC scores for any one domain are associated with lower function in that domain and lower QOL.
Thus higher symptom burden, which reflects both function and bother scores, translate into lower EPIC scores.
|
Baseline
|
|
The Expanded Prostate Cancer Index (EPIC) - Bowel Health
Time Frame: Baseline
|
The EPIC is a 26-item measure that assesses symptom burden in four domains: urinary symptoms, bowel symptoms, sexual symptoms and vitality.
Each domain has a subscale related to function and bother which together contribute to disease specific quality of life.
Each domain has a range of possible scores from 0 to 100, with lower scores indicating worse symptom burden.
Lower EPIC scores for any one domain are associated with lower function in that domain and lower QOL.
Thus higher symptom burden, which reflects both function and bother scores, translate into lower EPIC scores.
|
Baseline
|
|
The Expanded Prostate Cancer Index (EPIC) - Sexual Health
Time Frame: Baseline
|
The EPIC is a 26-item measure that assesses symptom burden in four domains: urinary symptoms, bowel symptoms, sexual symptoms and vitality.
Each domain has a subscale related to function and bother which together contribute to disease specific quality of life.
Each domain has a range of possible scores from 0 to 100, with lower scores indicating worse symptom burden.
Lower EPIC scores for any one domain are associated with lower function in that domain and lower QOL.
Thus higher symptom burden, which reflects both function and bother scores, translate into lower EPIC scores.
|
Baseline
|
|
The Expanded Prostate Cancer Index (EPIC) - General Health
Time Frame: Baseline
|
The EPIC is a 26-item measure that assesses symptom burden in four domains: urinary symptoms, bowel symptoms, sexual symptoms and vitality.
Each domain has a subscale related to function and bother which together contribute to disease specific quality of life.
Each domain has a range of possible scores from 0 to 100, with lower scores indicating worse symptom burden.
Lower EPIC scores for any one domain are associated with lower function in that domain and lower QOL.
Thus higher symptom burden, which reflects both function and bother scores, translate into lower EPIC scores.
|
Baseline
|
|
The Expanded Prostate Cancer Index (EPIC) - EPIC-26 Mean
Time Frame: Baseline
|
The EPIC is a 26-item measure that assesses symptom burden in four domains: urinary symptoms, bowel symptoms, sexual symptoms and vitality. Each domain has a subscale related to function and bother which together contribute to disease specific quality of life. Each domain has a range of possible scores from 0 to 100, with lower scores indicating worse symptom burden. Lower EPIC scores for any one domain are associated with lower function in that domain and lower QOL. Thus higher symptom burden, which reflects both function and bother scores, translate into lower EPIC scores. The EPIC-26 mean is the average of the five EPIC subscales. |
Baseline
|
|
The Expanded Prostate Cancer Index (EPIC) - Urinary Health, Irritative
Time Frame: 5 Months
|
The EPIC is a 26-item measure that assesses symptom burden in four domains: urinary symptoms, bowel symptoms, sexual symptoms and vitality.
Each domain has a subscale related to function and bother which together contribute to disease specific quality of life.
Each domain has a range of possible scores from 0 to 100, with lower scores indicating worse symptom burden.
Lower EPIC scores for any one domain are associated with lower function in that domain and lower QOL.
Thus higher symptom burden, which reflects both function and bother scores, translate into lower EPIC scores.
|
5 Months
|
|
The Expanded Prostate Cancer Index (EPIC) - Urinary Health, Obstructive
Time Frame: 5 Months
|
The EPIC is a 26-item measure that assesses symptom burden in four domains: urinary symptoms, bowel symptoms, sexual symptoms and vitality.
Each domain has a subscale related to function and bother which together contribute to disease specific quality of life.
Each domain has a range of possible scores from 0 to 100, with lower scores indicating worse symptom burden.
Lower EPIC scores for any one domain are associated with lower function in that domain and lower QOL.
Thus higher symptom burden, which reflects both function and bother scores, translate into lower EPIC scores.
|
5 Months
|
|
The Expanded Prostate Cancer Index (EPIC) - Bowel Health
Time Frame: 5 Months
|
The EPIC is a 26-item measure that assesses symptom burden in four domains: urinary symptoms, bowel symptoms, sexual symptoms and vitality.
Each domain has a subscale related to function and bother which together contribute to disease specific quality of life.
Each domain has a range of possible scores from 0 to 100, with lower scores indicating worse symptom burden.
Lower EPIC scores for any one domain are associated with lower function in that domain and lower QOL.
Thus higher symptom burden, which reflects both function and bother scores, translate into lower EPIC scores.
|
5 Months
|
|
The Expanded Prostate Cancer Index (EPIC) - Sexual Health
Time Frame: 5 Months
|
The EPIC is a 26-item measure that assesses symptom burden in four domains: urinary symptoms, bowel symptoms, sexual symptoms and vitality.
Each domain has a subscale related to function and bother which together contribute to disease specific quality of life.
Each domain has a range of possible scores from 0 to 100, with lower scores indicating worse symptom burden.
Lower EPIC scores for any one domain are associated with lower function in that domain and lower QOL.
Thus higher symptom burden, which reflects both function and bother scores, translate into lower EPIC scores.
|
5 Months
|
|
The Expanded Prostate Cancer Index (EPIC) - General Health
Time Frame: 5 Months
|
The EPIC is a 26-item measure that assesses symptom burden in four domains: urinary symptoms, bowel symptoms, sexual symptoms and vitality.
Each domain has a subscale related to function and bother which together contribute to disease specific quality of life.
Each domain has a range of possible scores from 0 to 100, with lower scores indicating worse symptom burden.
Lower EPIC scores for any one domain are associated with lower function in that domain and lower QOL.
Thus higher symptom burden, which reflects both function and bother scores, translate into lower EPIC scores.
|
5 Months
|
|
The Expanded Prostate Cancer Index (EPIC) - Urinary Health, Irritative
Time Frame: 12 Months
|
The EPIC is a 26-item measure that assesses symptom burden in four domains: urinary symptoms, bowel symptoms, sexual symptoms and vitality.
Each domain has a subscale related to function and bother which together contribute to disease specific quality of life.
Each domain has a range of possible scores from 0 to 100, with lower scores indicating worse symptom burden.
Lower EPIC scores for any one domain are associated with lower function in that domain and lower QOL.
Thus higher symptom burden, which reflects both function and bother scores, translate into lower EPIC scores.
|
12 Months
|
|
The Expanded Prostate Cancer Index (EPIC) - Urinary Health, Obstructive
Time Frame: 12 Months
|
The EPIC is a 26-item measure that assesses symptom burden in four domains: urinary symptoms, bowel symptoms, sexual symptoms and vitality.
Each domain has a subscale related to function and bother which together contribute to disease specific quality of life.
Each domain has a range of possible scores from 0 to 100, with lower scores indicating worse symptom burden.
Lower EPIC scores for any one domain are associated with lower function in that domain and lower QOL.
Thus higher symptom burden, which reflects both function and bother scores, translate into lower EPIC scores.
|
12 Months
|
|
The Expanded Prostate Cancer Index (EPIC) - Bowel Health
Time Frame: 12 Months
|
The EPIC is a 26-item measure that assesses symptom burden in four domains: urinary symptoms, bowel symptoms, sexual symptoms and vitality.
Each domain has a subscale related to function and bother which together contribute to disease specific quality of life.
Each domain has a range of possible scores from 0 to 100, with lower scores indicating worse symptom burden.
Lower EPIC scores for any one domain are associated with lower function in that domain and lower QOL.
Thus higher symptom burden, which reflects both function and bother scores, translate into lower EPIC scores.
|
12 Months
|
|
The Expanded Prostate Cancer Index (EPIC) - Sexual Health
Time Frame: 12 Months
|
The EPIC is a 26-item measure that assesses symptom burden in four domains: urinary symptoms, bowel symptoms, sexual symptoms and vitality.
Each domain has a subscale related to function and bother which together contribute to disease specific quality of life.
Each domain has a range of possible scores from 0 to 100, with lower scores indicating worse symptom burden.
Lower EPIC scores for any one domain are associated with lower function in that domain and lower QOL.
Thus higher symptom burden, which reflects both function and bother scores, translate into lower EPIC scores.
|
12 Months
|
|
The Expanded Prostate Cancer Index (EPIC) - General Health
Time Frame: 12 Months
|
The EPIC is a 26-item measure that assesses symptom burden in four domains: urinary symptoms, bowel symptoms, sexual symptoms and vitality.
Each domain has a subscale related to function and bother which together contribute to disease specific quality of life.
Each domain has a range of possible scores from 0 to 100, with lower scores indicating worse symptom burden.
Lower EPIC scores for any one domain are associated with lower function in that domain and lower QOL.
Thus higher symptom burden, which reflects both function and bother scores, translate into lower EPIC scores.
|
12 Months
|
|
Confidence in Symptom Self-Management
Time Frame: 5 months
|
Confidence in symptom self-management was measured using a 5-item scale developed from our pilot work.
Scores range from 5 to 15 with higher scores indicating higher level of confidence.
|
5 months
|
|
Confidence in Symptom Self-Management
Time Frame: 12 months
|
Confidence in symptom self-management was measured using a 5-item scale developed from our pilot work.
Scores range from 5 to 15 with higher scores indicating higher level of confidence.
|
12 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cancer Control
Time Frame: 5 months
|
We assessed perceived cancer control and outlook using five items from a validated measure developed to examine the psychosocial impact of prostate cancer.
This measure, the Measuring Patients' Perceptions of the Outcomes of Treatment for Early PC instrument by Clark et al., includes three domains related to confidence that one's cancer is under control, worries about recurrence, and appraisals of one's coping with PC.
Cancer control was assessed during the five- and 12-month follow-ups using two cancer control items from the instrument.
Scores range from 2 to 10 and higher scores indicate higher confidence that cancer is under control.
|
5 months
|
|
Cancer Control
Time Frame: 12 months
|
We assessed perceived cancer control and outlook using five items from a validated measure developed to examine the psychosocial impact of prostate cancer.
This measure, the Measuring Patients' Perceptions of the Outcomes of Treatment for Early PC instrument by Clark et al., includes three domains related to confidence that one's cancer is under control, worries about recurrence, and appraisals of one's coping with PC.
Cancer control was assessed during the five- and 12-month follow-ups using two cancer control items from the instrument.
Scores range from 2 to 10 and higher scores indicate higher confidence that cancer is under control.
|
12 months
|
|
Cancer Outlook
Time Frame: 5 months
|
We assessed perceived cancer control and outlook using five items from a validated measure developed to examine the psychosocial impact of prostate cancer.
This measure, the Measuring Patients' Perceptions of the Outcomes of Treatment for Early PC instrument by Clark et al., includes three domains related to confidence that one's cancer is under control, worries about recurrence, and appraisals of one's coping with PC.
Cancer outlook was assessed during the five- and 12-month follow-ups using three cancer outlook items from the instrument.
Scores range from 3 to 15 and higher scores indicate more positive cancer outlook.
|
5 months
|
|
Cancer Outlook
Time Frame: 12 months
|
We assessed perceived cancer control and outlook using five items from a validated measure developed to examine the psychosocial impact of prostate cancer.
This measure, the Measuring Patients' Perceptions of the Outcomes of Treatment for Early PC instrument by Clark et al., includes three domains related to confidence that one's cancer is under control, worries about recurrence, and appraisals of one's coping with PC.
Cancer outlook was assessed during the five- and 12-month follow-ups using three cancer outlook items from the instrument.
Scores range from 3 to 15 and higher scores indicate more positive cancer outlook.
|
12 months
|
|
Perceived Efficacy in Patient-Physician Interactions (PEPPI) - 5-item Short Form
Time Frame: 5 months
|
Self-efficacy in patient-physician interactions was assessed at 5 and 12 months using a five-item short form version of the Perceived Efficacy in Patient-Physician Interactions (PEPPI).
The PEPPI was developed to measure older patients' self-efficacy in obtaining medical information and attention to their medical concerns from physicians.
Scores range from 0-25 with higher scores indicating higher self-efficacy.
|
5 months
|
|
Perceived Efficacy in Patient-Physician Interactions (PEPPI) - 5-item Short Form
Time Frame: 12 months
|
Self-efficacy in patient-physician interactions was assessed at 5 and 12 months using a five-item short form version of the Perceived Efficacy in Patient-Physician Interactions (PEPPI).
The PEPPI was developed to measure older patients' self-efficacy in obtaining medical information and attention to their medical concerns from physicians.
Scores range from 0-25 with higher scores indicating higher self-efficacy.
|
12 months
|
|
Brief Cope - 6 Items
Time Frame: 5 months
|
We assessed participants' coping during the five- and 12-month follow-up assessments using six items from the 28-item Brief Cope instrument.
This instrument measures emotion-focused, problem-focused, and dysfunctional coping and has been used in cancer survivors.
Scores range from 1 to 5 with higher scores indicating better coping skills.
|
5 months
|
|
Brief Cope - 6 Items
Time Frame: 12 months
|
We assessed participants' coping during the five- and 12-month follow-up assessments using six items from the 28-item Brief Cope instrument.
This instrument measures emotion-focused, problem-focused, and dysfunctional coping and has been used in cancer survivors.
Scores range from 1 to 5 with higher scores indicating better coping skills.
|
12 months
|
|
Veteran Quality of Life Scale (VR-12) - Physical Health, 2 Items
Time Frame: 12 months
|
We assessed subjective physical health using 2 items from the VR-12 (SF-12 for veterans), an established measure of overall QOL that includes perceptions of one's health that may be impacted by prostate cancer.
The scores range from 1- 3 and higher scores correspond to better health.
|
12 months
|
|
Veteran Quality of Life Scale (VR-12) - Emotional Health, 3 Items
Time Frame: 12 months
|
We assessed subjective emotional health using 3 items from the VR-12 (SF-12 for veterans), an established measure of overall QOL that includes perceptions of one's health that may be impacted by prostate cancer.
The scores range from 1- 6 and higher scores correspond to better health.
|
12 months
|
Collaborators and Investigators
Investigators
- Principal Investigator: Sarah T Hawley, PhD MPH BA, VA Ann Arbor Healthcare System, Ann Arbor, MI
Publications and helpful links
General Publications
- Telem DA, Dimick J, Skolarus TA. Dissecting Surgeon Behavior: Leveraging the Theoretical Domains Framework to Facilitate Evidence-based Surgical Practice. Ann Surg. 2018 Mar;267(3):432-434. doi: 10.1097/SLA.0000000000002506. No abstract available.
- Skolarus TA, Wittmann D, Hawley ST. Enhancing prostate cancer survivorship care through self-management. Urol Oncol. 2017 Sep;35(9):564-568. doi: 10.1016/j.urolonc.2017.05.008. Epub 2017 Jun 13.
- Skolarus TA, Metreger T, Hwang S, Kim HM, Grubb RL 3rd, Gingrich JR, Hawley ST. Optimizing veteran-centered prostate cancer survivorship care: study protocol for a randomized controlled trial. Trials. 2017 Apr 18;18(1):181. doi: 10.1186/s13063-017-1925-4.
- Skolarus TA, Metreger T, Wittmann D, Hwang S, Kim HM, Grubb RL 3rd, Gingrich JR, Zhu H, Piette JD, Hawley ST. Self-Management in Long-Term Prostate Cancer Survivors: A Randomized, Controlled Trial. J Clin Oncol. 2019 May 20;37(15):1326-1335. doi: 10.1200/JCO.18.01770. Epub 2019 Mar 29.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IIR 12-116
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Prostate Cancer
-
Cancer Institute and Hospital, Chinese Academy...RecruitingProstate Cancer Castration-resistant Prostate CancerChina
-
Roswell Park Cancer InstituteRecruitingObesity | Overweight | Cancer Survivor | Prostate Adenocarcinoma | Stage I Prostate Cancer | Stage II Prostate Cancer | Stage III Prostate Cancer | Stage IV Prostate Cancer | Stage IIA Prostate Cancer | Stage IIB Prostate Cancer | Stage IVA Prostate Cancer | Stage IVB Prostate Cancer | Stage A Prostate Cancer | Stage... and other conditionsUnited States
-
Cancer Institute and Hospital, Chinese Academy...RecruitingProstate Cancer Castration-resistant Prostate CancerChina
-
Jonsson Comprehensive Cancer CenterProgenics Pharmaceuticals, Inc.TerminatedRandomized Trial of PSMA PET Scan Before Definitive Radiation Therapy for Prostate Cancer (PSMA-dRT)Stage II Prostate Cancer AJCC v8 | Stage IIIA Prostate Cancer AJCC v8 | Stage IIIB Prostate Cancer AJCC v8 | Stage IIC Prostate Cancer AJCC v8 | Stage III Prostate Cancer AJCC v8 | Stage IIIC Prostate Cancer AJCC v8 | Stage IIA Prostate Cancer AJCC v8 | Stage IIB Prostate Cancer AJCC v8 | Stage I Prostate...United States
-
Mayo ClinicNational Cancer Institute (NCI)WithdrawnStage I Prostate Cancer AJCC v8 | Stage II Prostate Cancer AJCC v8 | Stage IIIA Prostate Cancer AJCC v8 | Stage IIIB Prostate Cancer AJCC v8 | Stage IIC Prostate Cancer AJCC v8 | Stage III Prostate Cancer AJCC v8 | Stage IIIC Prostate Cancer AJCC v8 | Stage IIA Prostate Cancer AJCC v8 | Stage IIB Prostate...United States
-
Barbara Ann Karmanos Cancer InstituteGenentech, Inc.CompletedRecurrent Prostate Cancer | Stage I Prostate Cancer | Stage III Prostate Cancer | Adenocarcinoma of the Prostate | Stage IIA Prostate Cancer | Stage IIB Prostate CancerUnited States
-
Jonsson Comprehensive Cancer CenterNational Cancer Institute (NCI)CompletedRecurrent Prostate Cancer | Stage I Prostate Cancer | Stage III Prostate Cancer | Adenocarcinoma of the Prostate | Stage IV Prostate Cancer | Stage IIA Prostate Cancer | Stage IIB Prostate CancerUnited States
-
Ryan Kohlbrenner, MDRadiological Society of North AmericaCompletedProstate Adenocarcinoma | Stage IV Prostate Cancer AJCC v8 | Prostate Carcinoma | Stage IIIA Prostate Cancer AJCC v8 | Stage IIIB Prostate Cancer AJCC v8 | Stage IIC Prostate Cancer AJCC v8 | Stage III Prostate Cancer AJCC v8 | Stage IIIC Prostate Cancer AJCC v8 | Stage IVA Prostate Cancer AJCC v8 | Stage...United States
-
Sidney Kimmel Cancer Center at Thomas Jefferson...Regeneron Pharmaceuticals; Prostate Cancer FoundationWithdrawnStage III Prostate Cancer | Stage IV Prostate Cancer | Stage IVA Prostate Cancer | Stage IVB Prostate Cancer | Stage IIIA Prostate Cancer | Stage IIIB Prostate Cancer | Stage IIIC Prostate Cancer
-
University of Southern CaliforniaNational Cancer Institute (NCI); SanofiTerminatedDiarrhea | Recurrent Prostate Cancer | Hormone-resistant Prostate Cancer | Stage I Prostate Cancer | Stage III Prostate Cancer | Stage IV Prostate Cancer | Stage IIA Prostate Cancer | Stage IIB Prostate CancerUnited States
Clinical Trials on Interactive Voice Response Symptom Management
-
Ottawa Heart Institute Research CorporationHeart and Stroke Foundation of OntarioCompletedCoronary Artery DiseaseCanada
-
Michigan State UniversityNational Cancer Institute (NCI)CompletedMelanoma | Leukemia | Breast Neoplasms | Prostatic Neoplasms | Colorectal NeoplasmsUnited States
-
M.D. Anderson Cancer CenterCompleted
-
University of MichiganCompletedHypertensionHonduras, Mexico
-
M.D. Anderson Cancer CenterAmerican Cancer Society, Inc.Completed
-
M.D. Anderson Cancer CenterCompletedLung CancerUnited States
-
M.D. Anderson Cancer CenterCompletedEsophageal Cancer | Lung CancerUnited States