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Feasibility study of cancer rehabilitation during concurrent chemoradiation for cervical cancer

Feasibility study of cancer rehabilitation during concurrent chemoradiation for cervical cancer - Cancer rehabilitation during concurrent chemoradiation for cervical cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000034498
Enrollment
20
Registered
2018-10-15
Start date
2018-10-15
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

cervical cancer

Interventions

Perform stretching, strength training, balance practice, endurance training for 20 minutes 4 times a week. Weekends, holidays and the day of chemotherapy were excluded.

Sponsors

Department of Obstetrics and Gynecology Kurume University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Patients who got written consent. 2. Over 20 years old 3. Patients who recieve CCRT under hospitalization for the diagnosis of cervical cancer

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
Implementation rate of rehabilitation

Secondary

MeasureTime frame
safety body function (muscle srength, body composition, lower limb circumference, balance ability, walking ability) Change of quality of life and fatigue Adverse event and treatment completion rate of CCRT Identification of factors related to completion of rehabilitation

Countries

Japan

Contacts

Public ContactKazuto Tasaki

Kurume University Obstetrics and Gynecology

kazzvic@yahoo.co.jp0942-31-7573

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026