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Evaluation of Needs of Patients and Care-givers During and After Radiotherapy of Patients With Prostate Cancer (PrähabPro)

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Charité University Medicine Berlin

Status

Enrolling

Conditions

Prostate Cancer Patients

Treatments

Other: Interview

Study type

Interventional

Funder types

Other

Identifiers

NCT07156903
EA4/121/25

Details and patient eligibility

About

Exploratory qualitative survey to assess the needs of patients and their relatives during and after radiotherapy for prostate cancer and their attitudes and wishes regarding prehabilitation measures

Full description

Across Germany, more than 500,000 people are newly diagnosed with cancer each year (Center for Cancer Registry Data, RKI, 2020). Prostate cancer, the most common cancer in men, affects more than 65,000 patients annually (https://www.krebsinformationsdienst.de/prostatakrebs). The gold standard for the treatment of advanced prostate cancer is radiotherapy combined with anti-hormonal therapy. If the cancer is detected earlier, surgery can be performed. Both procedures are then considered to be oncologically equivalent. Despite the most modern treatment methods and techniques, severe acute and long-term side effects still occur, which patients can experience as extremely limiting. These include, among other things, loss of libido and erectile function, the development of bladder weakness and even incontinence, and changes in bowel function (e.g., diarrhea).

Currently, patients often only begin treatments designed to mitigate these side effects during their rehabilitation, at least 4-6 weeks after therapy. However, the investigators believe that greater effects can be achieved and even the occurrence of serious side effects can be potentially prevented if treatment is initiated before or during therapy. This concept is called prehabilitation.

In order to develop a suitable prehabilitation program for prostate cancer patients undergoing curative radiation therapy (either definitive or postoperative), the investigators will conduct interviews with patients and, if possible, their immediate family members (e.g., partners) to learn more about their experiences before, during, and after the treatment. The investigators would also like to learn more about their attitudes and wishes regarding prehabilitation measures.

Enrollment

60 estimated patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosed Prostate Cancer with curativ intended Radiotherapy
  • min. 18 years
  • sufficient knowledge of German language for participation in interviews
  • Capacity to consent

Exclusion criteria

  • age <18 years

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

60 participants in 1 patient group

interviews
Experimental group
Description:
Patients will be asked to participate in interviews
Treatment:
Other: Interview

Trial contacts and locations

1

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Central trial contact

Franziska Hausmann, MD

Data sourced from clinicaltrials.gov

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