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Influence of targeted exercise therapy on quality of life in patients after condition with peri- and postoperative uveamelanoma.

Influence of targeted exercise therapy on quality of life in patients after condition with peri- and postoperative uveamelanoma. - EyeCanMoveiT

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
DRKS
Registry ID
DRKS00031207
Enrollment
75
Registered
2023-02-03
Start date
2023-01-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

C69

Interventions

Group 1: A total of 6 weeks (á 2 times per week), in total 12 units, 2 weeks pre-operative and 4 weeks post-operative, supervised exercise therapy performed by qualified exercise therapists. Each sess

Sponsors

Universitätsklinikum Köln
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Diagnosis of uveamelanoma; prior to first-line oncologic therapy, radiotherapy (cyberknife) or enucleation; curative medical treatment approach or life expectancy at least 6 months; good German language skills; written informed consent.

Exclusion criteria

Exclusion criteria: - Failure to meet inclusion criteria - Shortened life expectancy of less than 6 months - All general diseases that do not allow sports activity in particular: o Clinical-manifest heart failure (NYHA III-IV). o Respiratory partial or global insufficiency o Permanent thrombocytopenia <10,000/µl, e.g., refractory autoimmune thrombocytopenia o Congenital or acquired thrombocytopathies or coagulation disorders. o Symptomatic CHD (clearance certificate required, stress ECG and cardiac ultrasound recommended if necessary) o Severe refractory hypertension o Uncontrollable COPD o Uncontrolled cerebral seizure disorder o Severe anemia (requiring transfusion). - Medical or mental condition that, in the opinion of the investigator, does not allow the patient to participate in the study or provide a legally binding signature on the informed consent form - Lack of willingness to store and share personal medical records as part of the protocol - Participation in another exercise therapy study

Design outcomes

Primary

MeasureTime frame
Health-related quality of life

Secondary

MeasureTime frame
- Hand-eye coordination - Endurance capacity - Static and dynamic balance - Movement behavior/physical activity - Psychological well-being (anxiety and depression) - Neck pain - Employment and financial status

Countries

Germany

Contacts

Public ContactFreerk T. Baumann

Universitätsklinikum Köln

freerk.baumann@uk-koeln.de+49221 478-42643

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 9, 2026