Feasibility study of cancer rehabilitation during concurrent chemoradiation for cervical cancer

Not Applicable

• Conditions: cervical cancer

• Registration Number: JPRN-UMIN000034498
• Lead Sponsor: Department of Obstetrics and Gynecology Kurume University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-10-15
• Study Completion: 2020-07-31
• Last Update Posted: 20 November 2023

Recruitment & Eligibility

• Status: Complete: follow-up continuing
• Sex: Female
• Target Recruitment: 20

Inclusion Criteria

Not provided

Exclusion Criteria

1. PS 3,4 2. Patients who need assistance in walking 3. Patients who have difficulty understanding instruction by language 4. Patients with complications affecting walking 5. Patient who is difficult to fill in questionnaire 6. Restriction of rest by bone lesion, cases where evaluation cooperation can not be obtained due to remarkable pain 7. Blood findings: Hb 7.5 g/dL or less, Plt 20,000/uL or less, WBC 3,000/uL or less 8. Invasion of more than 50% of the bone cortex, bone erosion towards the center of the bone, metastatic findings of the long bone with 3 cm or more lesions of the femur 9. Cavity internal organs, blood vessels, compression of the spinal cord 10. Pain, dyspnea, exudate retention in the pleura, pericardium, retroperitoneum with movement restriction 11. Dysfunction of the central nervous system, disturbance of consciousness, hypercranial hypertension 12. hypokalemia, hyperkalemia, hyponatremia, hypernatremia, hypocalcemia, hypercalcemia 13. Orthostatic hypotension, hypertension of 160/100 mmHg or more 14. Tachycardia of 110/min or more, ventricular arrhythmia

Study & Design

• Study Type: Interventional
• Study Design: Not specified