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Influences of targeted exercise therapy on treatment-related side effects of hormonetherapy in prostate cancer patients

Influences of targeted exercise therapy on treatment-related side effects of hormonetherapy in prostate cancer patients - Burgdorf-Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00009975
Enrollment
60
Registered
2016-02-09
Start date
2016-02-10
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

C61

Interventions

Group 1: Strength-endurance training: 2x per week supervised about 75min, warming-up, 7 different strength exercises (2-4 series á 8-12 repetitions at 75 % of 1RM) + impact-training, cooling-down Grou

Sponsors

Deutsche Sporthochschule zu Köln
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Prostate cancer patients who have received hormone therapy continuously at least over a period of 3 months and a maximum of 12 months. The treatment needs to be continue for at least one year. Half of the patients ( n = 30) received Leuprone® , the other half ( n = 30) alternative hormonal therapies. Serum testosterone levels 18 singed informed consent

Exclusion criteria

Exclusion criteria: ongoing medication with tricyclic antidepressants and duloxetine (Yentreve) WHO / ECOG performance status> 2 Planned OP Life expectancy <6 months All disease situations that do not allow a sporting activity, in particular: Clinically manifest heart failure (NYHA III-IV) Respiratory partial or global failure Durable thrombocytopenia <10,000 / ul, for example, Autoimmunthrombozytopenien intractable. Congenital or acquired thrombocytopenia or any coagulation disorder. Symptomatic CHD (possibly performing exercise ECG is recommended) Severe intractable hypertension Not adjustable COPD Uncontrolled cerebral convulsions CNS metastases Medical or mental state that leads the investigator to not allowing the patient to participate in the study. or a legally binding signature of the consent form does Unwillingness to storage and transfer of personal data in the context of the study protocol. Participation in another sport-study

Design outcomes

Primary

MeasureTime frame
Strength: dynamically on a isokinetic dynamometer Measurements: Baseline, 3, 6 and 12 months, and 6 and 12 months follow-up

Secondary

MeasureTime frame
Endurance with a 30/15 Test on a bicycle ergometer Quality of life via a questionnaire (EORTC QLQ - C30 and PR25) Fatigue via a questionnaire (MFI) Body composition via BIA (bioelectrical impedance analysis) erectile dysfunction via a questionnaire (IIEF) bone pain via a questionnaire (FACT- BP) Activity level via questionnaires (QPAQ and KAS ) BMI BMD via DXA scan PSA and testosterone value Measurement timing: See primary endpoint, except bone density BMD measurements: baseline, after 12 months and 12 months follow -up

Countries

Germany

Contacts

Public ContactAnja Großek

Deutsche Sporthochschule Köln, Institut für Kreislaufforschung und Sportmedizin

a.grossek@dshs-koeln.de0221 4982 5450

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 19, 2026