Staying Strong and Healthy During Androgen Deprivation Therapy (ADT) for Men

Sponsor
University of Kansas Medical Center (Other)
Overall Status
Completed
CT.gov ID
NCT02969577
Collaborator
National Institute of Nursing Research (NINR) (NIH)
38
2
2
40.8
19
0.5

Study Details

Study Description

Brief Summary

The purpose of this study is to learn if lifestyle changes and counseling along with standard medical care, compared to standard medical care alone, can prevent heart problems and diabetes in men who are receiving ADT for prostate cancer treatment.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Exercise Program
  • Behavioral: Diet and Nutrition Coaching
  • Other: Usual Care with Attention
N/A

Detailed Description

Prostate cancer is a very treatable cancer but those treatments can have long-lasting effects. A kind of hormone therapy called Androgen Deprivation Therapy (ADT) is often used along with other treatments like radiation and has been shown to improve survival. However, ADT can have negative effects especially on the heart and metabolism (the body's system for using and storing energy).

Participation in this study will last for up to 12 months. The study is looking at two different approaches to treating men who are undergoing ADT:

  1. Staying Strong & Healthy Intervention + Usual Care

  2. Usual Care

All participants will have blood drawn and be asked questions about how they are feeling during their participation. The men in the Staying Strong & Healthy Intervention group will also take part in a diet and exercise program and receive counseling from a member of the study team.

Study Design

Study Type:
Interventional
Actual Enrollment :
38 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Staying Strong and Healthy During Androgen Deprivation Therapy (ADT) for Men
Actual Study Start Date :
Mar 7, 2017
Actual Primary Completion Date :
Jul 1, 2020
Actual Study Completion Date :
Jul 31, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Staying Strong & Healthy Intervention (SS&H)

Participants will take part in a 6-month exercise program and diet and nutrition coaching program. Also part of this arm is a nutritional and lifestyle counseling program to be lead by a member of the study team. Participants will also receive the usual care they would normally receive if not taking part in this study.

Behavioral: Exercise Program
Participants will have a personal training session at the first visit. A member of the study team will discuss strength training and cardiovascular workouts for them to complete over the first 6 months of the study. A member of the study team will then talk with the participant every week for the first 3 months and monthly afterwards until month 6. Participants will be sent exercise videos and be given recommendations for the exercise program via phone calls and will be tailored to the individual. Videos and recommendations will be sent directly to the participant's smartphone.

Behavioral: Diet and Nutrition Coaching
Diet and nutrition coaching session with an overview of resources on the smartphone. Over the first 6 months, participants will receive healthy recipes and nutritional information on the smartphone.

Other: Usual Care with Attention
Participants will receive the usual care for men undergoing ADT. This includes monitoring blood work and answering questions about how they are feeling. Participants will be directed to the IMPACT website for education materials on prostate cancer.

Active Comparator: Usual Care with Attention (UCA)

Participants will receive the usual care they would normally receive if not taking part in this study.

Other: Usual Care with Attention
Participants will receive the usual care for men undergoing ADT. This includes monitoring blood work and answering questions about how they are feeling. Participants will be directed to the IMPACT website for education materials on prostate cancer.

Outcome Measures

Primary Outcome Measures

  1. Change in LDL [Change from Baseline to Month 12]

Secondary Outcome Measures

  1. Change in Body Mass Index (BMI) [Change from Baseline to Month 6]

  2. Change in Body Mass Index (BMI) [Change from Baseline to Month 12]

  3. Change in Lipid Profile [Change from Baseline to Month 6]

  4. Change in Lipid Profile [Change from Baseline to Month 12]

  5. Change in Waist/Hip Circumference [Change from Baseline to Month 6]

  6. Change in Waist/Hip Circumference [Change from Baseline to Month 12]

  7. Change in Glucose [Change from Baseline to Month 6]

  8. Change in Glucose [Change from Baseline to Month 12]

  9. Change in Health Related Quality [Change from Baseline to Month 6]

    Quality of life will be measured using the SF-12 and Expanded Prostate Cancer Index Composite. The two are scored together and result in a composite score. Scores can range from 0-100. The higher the score the better the quality of life.

  10. Change in Health Related Quality [Change from Baseline to Month 12]

    Quality of life will be measured using the SF-12 and Expanded Prostate Cancer Index Composite. The two are scored together and result in a composite score. Scores can range from 0-100. The higher the score the better the quality of life.

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years and Older
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Diagnosed with prostate cancer

  • Starting or have started ADT (oral or injection) for prostate cancer treatment within the last 3 months

  • Re-initiating ADT after being on holiday for longer than their ADT dosage (e.g. If the man's dosage is every six months and he has been off ADT for more than six he is eligible);

  • Able to speak and read in English or Spanish

  • Reachable consistently by telephone

  • Able to travel to KUMC

Exclusion Criteria:
  • Not diagnosed with prostate cancer

  • Not receiving or planning to receive ADT for prostate cancer treatment within the last three months

  • Initiating ADT for prostate cancer prior to the previous 3 months or are not on ADT holiday

  • Not able to speak and read in English or Spanish

  • Not reachable consistently by telephone

  • Not able to travel to the study site for data collection

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of California, Los Angeles Los Angeles California United States 90095
2 University of Kansas Medical Center Kansas City Kansas United States 66160

Sponsors and Collaborators

  • University of Kansas Medical Center
  • National Institute of Nursing Research (NINR)

Investigators

  • Principal Investigator: Sally Maliski, PhD, RN, FAAN, University of Kansas Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Kansas Medical Center
ClinicalTrials.gov Identifier:
NCT02969577
Other Study ID Numbers:
  • STUDY00004205
  • R01NR014518
First Posted:
Nov 21, 2016
Last Update Posted:
Feb 17, 2021
Last Verified:
Feb 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Kansas Medical Center
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 17, 2021