Exercise and Cognitive-psychosocial Functions in Men With Prostate Cancer Receiving Androgen Depletion Therapy

Not Applicable

Completed

• Conditions: Prostate Cancer
• Interventions: Behavioral: Exercise; Behavioral: Control

• Registration Number: NCT00856102
• Lead Sponsor: University of Manitoba

Brief Summary

The objective of the proposed research is to determine the efficacy of a home-based walking exercise program in promoting cognitive-psychosocial functions of men with prostate cancer receiving androgen depletion therapy (ADT). ADT is the mainstay treatment for men with advanced prostate cancer. However, ADT has a number of side effects including compromised cognitive function, depression and anxiety, which negatively impacts the quality of life of men with prostate cancer. The central question of the proposed research is to determine if exercise will have a positive impact on the quality of life of men with prostate cancer undergoing ADT.

Hypothesis:

Detailed Description

Not available

Study Timeline

• Study Start: 2009-03
• Study First Submitted: 2009-03-03
• Study First Submitted QC: 2009-03-03
• Study First Posted: 2009-03-05
• Primary Completion: 2010-12
• Study Completion: 2010-12
• Status Verified: 2011-01
• Last Update Submitted: 2011-01-31
• Last Update Posted: 2011-02-01

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Male
• Target Recruitment: 30

Inclusion Criteria

• men aged 50 or older
• diagnosed with adenocarcinoma prostate cancer
• will initiate and receive continuous ADT (LHRH or combination of LHRH and anti-androgen for at least 6 months

Exclusion Criteria

• severe cardiac disease (New York Heart Association class III or greater)
• angina
• severe osteoporosis
• uncontrolled hypertension
• orthostastic blood pressure drop > 20mm Hg
• moderate to severe aortic stenosis
• acute illness or fever
• uncontrolled atrial or ventricular dysrhythmias
• uncontrolled sinus tachycardia (> 120 beats per minute)
• uncontrolled congestive heart failure
• third-degree atrio-ventricular heart block
• active pericarditis or myocarditis
• recent embolism, thrombophlebitis
• deep vein thrombosis, resting ST displacement
• uncontrolled diabetes
• uncontrolled pain
• cognitive impairment
• history of falls due to balance impairment or lost of consciousness
• severe neuromusculoskeletal conditions that limit their ability to perform walking exercise

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Exercise	Exercise	-
Control	Control	-

Primary Outcome Measures

Name	Time	Method
Cognitive-psychosocial functions	3 and 6 months

Secondary Outcome Measures

Name	Time	Method
health-related quality of life	3 and 6 months

Trial Locations

Locations (1)

University of Manitoba; 🇨🇦 Winnipeg, Manitoba, Canada