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临床试验/NCT02036684
NCT02036684已完成1 期

A Multicentre, Pilot Randomized Controlled Trial to Examine the Effects of Prehabilitation on Functional Outcomes After Radical Prostatectomy

University of Guelph-Humber4 个研究点 分布在 1 个国家目标入组 86 人开始时间: 2013年11月最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
86
试验地点
4
主要终点
Contamination

研究概览

简要总结

Radical prostatectomy is the most common and effective treatment for localized prostate cancer. Unfortunately, radical prostatectomy is associated with significant adverse effects, such as urinary incontinence, sexual dysfunction, and reduced physical function that collectively diminish health-related quality of life which may persist for up to two years postoperatively. The primary objective of this trial is to assess the feasibility of conducting of a multi-site randomized controlled trial to test the effect of a comprehensive prehabilitation program versus standard care for men with prostate cancer undergoing radical prostatectomy. We hypothesize that men with prostate cancer undergoing radical prostatectomy in the comprehensive prehabilitation program (full-body exercises and pelvic floor muscle exercises) will report better health-related quality of life, urological symptoms, and physical fitness, physical activity, and pain, as well as a shorter postoperative length of stay than participants receiving standard preoperative care (pelvic floor muscle exercises alone). Our secondary objective is to report estimates of efficacy on several clinically important outcomes for this population that will be used for sample size calculations in an adequately powered trial.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
40 Years 至 80 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Men with localized prostate cancer (stage cT1- cT2) who have consented for radical prostatectomy
  • between the ages of 40 and 80 years.

排除标准

  • i) severe coronary artery disease (Canadian Cardiovascular Society class III or greater);
  • ii) significant congestive heart failure (New York Heart Association class III or greater);
  • iii) uncontrolled pain;
  • iv) neurological or musculoskeletal co-morbidity inhibiting exercise;
  • v) diagnosed psychotic, addictive, or major cognitive disorders;
  • vi) no more than two of the following Coronary Risk Factors as defined by the American College of Sports Medicine : family history of coronary disease, cigarette smoking, hypertension (SBP > 140 mmHg; DBP > 90 mmHg), known dyslipidemia, known impaired fasting, glucose (>110 mg/dL), obesity (BMI > 30 kg/m2 or waist circumference > 102cm), or physically inactive (<150 min of moderate intensity physical activity per week).

结局指标

主要结局

Contamination

时间窗: 26 weeks postoperatively

The same exercise logbook questions that ask about aerobic and resistance exercise, and pelvic floor muscle exercises, will be administered to both groups to assess contamination.

Study Retention

时间窗: 26 weeks postoperatively

Retention will be assessed by measuring attrition throughout the intervention period and at each assessment.

Recruitment

时间窗: When recruitment is complete (approximately 12 months after study initiation; January 2015)

Prior exercise trials in prostate cancer patients on hormone and/or radiation therapy have observed recruitment rates of 25-40%, but no studies have assessed recruitment to a preoperative exercise intervention among prostate cancer survivors. We will measure recruitment-success percentage and will record reasons for non-participation to better understand why men electing radical prostatectomy would not participate in an exercise intervention.

Adherence to Prehabilitation Program

时间窗: 26 weeks postoperatively

Adherence to the home-based exercise program (aerobic and resistance) and pelvic floor muscle exercises will be measured through a logbook completed by the research coordinator during weekly communication.

次要结局

  • Quality of Life(At baseline, within 1 week prior to surgery, and at 4, 12, and 26 weeks postoperatively.)
  • Psychosocial Wellbeing(At baseline, within 1 week prior to surgery, and at 4, 12, and 26 weeks postoperatively.)
  • Length of stay(From time of surgery to discharge (typically 1 week))
  • Physical Fitness(At baseline, within 1 week prior to surgery, and at 4, 12, and 26 weeks postoperatively.)
  • Physical Activity(At baseline, within 1 week prior to surgery, and at 4, 12, and 26 weeks postoperatively.)
  • Treatment Complications(26 weeks postoperatively)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Daniel Santa Mina

Program Head

University of Guelph-Humber

研究点 (4)

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