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Behavior-Based Dietary Intervention in Treating Patients With Hormone-Refractory Prostate Cancer

Primary Purpose

Prostate Cancer

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
behavioral dietary intervention
dietary intervention
therapeutic dietary intervention
Sponsored by
M.D. Anderson Cancer Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer focused on measuring stage I prostate cancer, stage II prostate cancer, adenocarcinoma of the prostate

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)MaleDoes not accept healthy volunteers

DISEASE CHARACTERISTICS: Histologically confirmed adenocarcinoma of the prostate No small cell component No histologically confirmed and/or demonstrable metastatic or locally recurrent disease by bone scan, chest x-ray, computed tomography (CT) scan, or transrectal ultrasound No clinical symptoms within the past 90 days Documented biochemical failure after radical prostatectomy Prostate-specific antigen must have initially nadired to an undetectable level (< 0.1 ng/mL) after prostatectomy AND is currently rising (0.3-40.0 ng/mL) Serum testosterone > 100 ng/dL PATIENT CHARACTERISTICS: Age Any age Performance status Zubrod 0-1 Life expectancy At least 1 year Hematopoietic Not specified Hepatic Not specified Renal Not specified Other No known allergic reactions to milk or soy products PRIOR CONCURRENT THERAPY: Biologic therapy Not specified Chemotherapy More than 1 year since prior chemotherapy Endocrine therapy More than 1 year since prior hormonal therapy Radiotherapy Not specified Surgery See Disease Characteristics

Sites / Locations

  • University of Texas - MD Anderson Cancer Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Arm I: Dietary Intervention

Arm II: Observation

Arm Description

Nutritional counseling on a low-fat, high-fiber, soy supplemented diet and behavior-based activities, such as goal-setting, contracting, and stimulus control, once weekly for 6 weeks, every 3 weeks for 33 weeks, and then at weeks 44, 48, and 52.

Observation every 6 weeks for 36 weeks and then every 8 weeks for 18 weeks.

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
May 14, 2004
Last Updated
November 5, 2018
Sponsor
M.D. Anderson Cancer Center
Collaborators
National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT00082732
Brief Title
Behavior-Based Dietary Intervention in Treating Patients With Hormone-Refractory Prostate Cancer
Official Title
Impact of Dietary Intervention in Men With Hormone Refractory Prostate Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
November 2018
Overall Recruitment Status
Completed
Study Start Date
July 28, 2000 (Actual)
Primary Completion Date
February 27, 2006 (Actual)
Study Completion Date
February 27, 2006 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
M.D. Anderson Cancer Center
Collaborators
National Cancer Institute (NCI)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
RATIONALE: A low-fat, high-fiber diet that includes soy protein may prevent disease progression in patients with hormone-refractory prostate cancer. Nutrition counseling may help motivate patients to follow this diet. PURPOSE: Randomized phase I trial to study the effectiveness of behavior-based dietary interventions, such as receiving nutrition counseling, in helping patients who have hormone-refractory prostate cancer follow a low-fat, high-fiber, soy-supplemented diet.
Detailed Description
OBJECTIVES: Determine whether a behavior-based dietary intervention can motivate patients with hormone-refractory prostate cancer to adopt and maintain a dietary pattern that includes < 20% of energy from fat, > 25 g of fiber, and 80 g of soy protein powder. Compare bioavailable levels of testosterone in patients treated with a behavior-based dietary intervention vs observation only. Determine whether this dietary intervention decreases or stabilizes a rising serum prostate-specific antigen level in these patients. Determine whether this dietary intervention improves disease-specific survival, mediated by reduced bioavailable levels of testosterone, in these patients. Determine the impact of a positive intervention outcome on androgen receptors in patients treated with this dietary intervention. OUTLINE: This is a randomized, controlled, pilot, multicenter study. Patients are randomized to 1 of 2 treatment arms. All patients receive nutritional counseling on a healthy diet. Patients also keep a food diary during study participation. Arm I (dietary intervention): Patients receive dietary intervention comprising nutritional counseling on a low-fat, high-fiber, soy supplemented diet and behavior-based activities, such as goal-setting, contracting, and stimulus control, once weekly for 6 weeks, every 3 weeks for 33 weeks, and then at weeks 44, 48, and 52. Treatment continues in the absence of disease progression or unacceptable toxicity. Arm II (observation): Patients undergo observation every 6 weeks for 36 weeks and then every 8 weeks for 18 weeks. PROJECTED ACCRUAL: A total of 92 patients (46 per treatment arm) will be accrued for this study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
stage I prostate cancer, stage II prostate cancer, adenocarcinoma of the prostate

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
56 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm I: Dietary Intervention
Arm Type
Experimental
Arm Description
Nutritional counseling on a low-fat, high-fiber, soy supplemented diet and behavior-based activities, such as goal-setting, contracting, and stimulus control, once weekly for 6 weeks, every 3 weeks for 33 weeks, and then at weeks 44, 48, and 52.
Arm Title
Arm II: Observation
Arm Type
No Intervention
Arm Description
Observation every 6 weeks for 36 weeks and then every 8 weeks for 18 weeks.
Intervention Type
Behavioral
Intervention Name(s)
behavioral dietary intervention
Intervention Type
Dietary Supplement
Intervention Name(s)
dietary intervention
Intervention Type
Procedure
Intervention Name(s)
therapeutic dietary intervention

10. Eligibility

Sex
Male
Accepts Healthy Volunteers
No
Eligibility Criteria
DISEASE CHARACTERISTICS: Histologically confirmed adenocarcinoma of the prostate No small cell component No histologically confirmed and/or demonstrable metastatic or locally recurrent disease by bone scan, chest x-ray, computed tomography (CT) scan, or transrectal ultrasound No clinical symptoms within the past 90 days Documented biochemical failure after radical prostatectomy Prostate-specific antigen must have initially nadired to an undetectable level (< 0.1 ng/mL) after prostatectomy AND is currently rising (0.3-40.0 ng/mL) Serum testosterone > 100 ng/dL PATIENT CHARACTERISTICS: Age Any age Performance status Zubrod 0-1 Life expectancy At least 1 year Hematopoietic Not specified Hepatic Not specified Renal Not specified Other No known allergic reactions to milk or soy products PRIOR CONCURRENT THERAPY: Biologic therapy Not specified Chemotherapy More than 1 year since prior chemotherapy Endocrine therapy More than 1 year since prior hormonal therapy Radiotherapy Not specified Surgery See Disease Characteristics
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Richard J. Babaian, MD
Organizational Affiliation
M.D. Anderson Cancer Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Texas - MD Anderson Cancer Center
City
Houston
State/Province
Texas
ZIP/Postal Code
77030-4009
Country
United States

12. IPD Sharing Statement

Links:
URL
http://www.mdanderson.org
Description
MD Anderson Cancer Center official website

Learn more about this trial

Behavior-Based Dietary Intervention in Treating Patients With Hormone-Refractory Prostate Cancer

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