DRKS00031854尚未招募Unknown
Establishment of a prehabilitation process for patients with prostate cancer prior to curatively intended radical prostatectomy - an exploratory, prospective, controlled intervention study. - PreHab
Klinik und Poliklinik für Urologie und Kinderurologie Universitätsklinikum Bonn0 个研究点目标入组 252 人开始时间: 2023年9月22日最近更新:
适应症
试验速览
- 阶段
- Unknown
- 状态
- 尚未招募
- 发起方
- 入组人数
- 252
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized controlled study
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 85 Years(—)
- 性别
- Male
入选标准
- •Patients who meet the following criteria may be included in the study:
- •Patients are between = 18 and = 85 years of age.
- •The patient has histologically confirmed prostate carcinoma.
- •The indication for radical prostatectomy is present and the patient wishes to undergo this procedure.
- •The patient is physically fit to participate in the planned procedures at the discretion of the investigator.
- •At the discretion of the investigator, the patient is mentally capable of understanding the consequences of participation in the study and can adequately evaluate the resulting obligations.
- •The patient gives written documented consent to study participation and the written documented informed consent form is available.
- •The patient is able to follow the study instructions and is likely to attend all required study visits (compliance).
- •The patient has the physical and cognitive ability to perform the physical training and participate in the psycho-oncology sessions, at the discretion of the investigator
- •The patient has the physical and cognitive ability to handle digital media and play internet videos, e.g., for whole body fitness training.
- •The patient has internet access and appropriate hardware to participate in the whole-body fitness training or to ensure transmission of data from the fitness watch vívosmart® 4 (by Garmin).
排除标准
- •Patients who meet any of the following criteria will not be included in the study:
- •The patient has a BMI > 40.
- •The patient is concurrently participating in another clinical trial or has participated in a clinical trial within the last 30 days that involved the use of an investigational drug.
- •The patient is or has been, to the knowledge or at the discretion of the investigator, dependent on medication, drugs, or alcohol.
研究者
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