C44.1
Conditions
Interventions
Group 1: Eye cancer patients who are about to undergo medical treatment for removal of basal cell carcinoma of the eyelid followed by temporary closure of one eye (Hughes' plastic) will be followed ov
Sponsors
Universitätsklinikum Köln
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - Diagnosis of basal cell carcinoma - Age = 18 years - Prior to surgical excision followed by eyelid reconstruction using Hughes' plastic surgery - Curative medical treatment approach or life expectancy at least 6 months - Good German language skills - Signed 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: - Clinically-manifest heart failure (NYHA III-IV). - Respiratory partial or global insufficiency - Permanent thrombocytopenia <10,000/µl, e.g., refractory autoimmune thrombocytopenia - Congenital or acquired thrombocytopathies or coagulation disorders. - Symptomatic CHD (clearance certificate required, stress ECG and cardiac ultrasound recommended if necessary) - Severe refractory hypertension - Uncontrollable COPD - Uncontrolled cerebral seizure disorder - 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 disease data as part of the protocol - Participation in another exercise therapy study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Testing will occur at 5 time points: Immediately before medical intervention, surgical eye closure (t0), immediately after medical intervention (t1), immediately before eye opening (t2), three weeks after opening (t3), and 6-month follow-up (t4). The primary endpoint, hand-eye coordination, will be assessed using the Purdue Pegboard Test (Lafayette Instruments, USA) | — |
Secondary
| Measure | Time frame |
|---|---|
| - Health-related quality of life - Indication-specific health-related quality of life - Endurance capacity - Static and dynamic balance - Movement behavior/physical activity - Psychological well-being (depression and anxiety) - Neck pain - Employment and financial status | — |
Countries
Germany
Contacts
Public ContactFreerk T. Baumann
Universitätsklinikum Köln
Outcome results
None listed