Skip to content

A Pilot Feasibility Study of an Online-based Exercise Program for Outpatients with Cancer

A Single-arm, Open-label Pilot Study to Evaluate the Feasibility of an Online-based Exercise Intervention for Outpatients with Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1030260146
Enrollment
15
Registered
2026-05-21
Start date
2026-05-21
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

cancer

Interventions

Single-arm, open-label, 8-week telerehabilitation exercise program for outpatients with cancer, delivered remotely by a physical or occupational therapist experienced in cancer rehabilitation. The pro
online, exercise, physical therapist, occupational therapist

Sponsors

Kinkawa Junya
Lead Sponsor
Kinkawa Junya
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Eligible patients must meet ALL of the following: 1. Histologically or cytologically confirmed diagnosis of any type of cancer. 2. Clinical stage I or higher. 3. Currently undergoing outpatient cancer treatment, or in an active follow-up phase within 5 years after diagnosis (regular imaging or blood tests at least once a year). 4. Aged 18 years or older at the time of informed consent. 5. ECOG Performance Status 0 to 2 and Karnofsky Performance Status 60% or higher. 6. Owns and is willing/able to use an ICT device (smartphone or tablet). 7. Has a safe space at home (or equivalent) for exercise: no protruding objects within 1.5 m radius, with a stable chair or wall available for support. 8. Able to communicate effectively in Japanese. 9. Provides written informed consent of their own free will.

Exclusion criteria

Exclusion criteria: Patients meeting any of the following will be excluded: 1. Estimated life expectancy of less than 3 months. 2. Diagnosed with terminal cancer and currently receiving primarily palliative home nursing care. 3. Any absolute contraindication to the intervention, including but not limited to: unstable angina or recent myocardial infarction (within 3 months); uncontrolled hypertension (resting SBP >180 mmHg or DBP >110 mmHg); severe aortic stenosis; acute systemic illness or fever; uncontrolled arrhythmia causing symptoms or hemodynamic instability; known meningeal carcinomatosis; spinal cord compression due to vertebral metastases with widespread advanced disease. 4. Severe cognitive impairment that prevents understanding of instructions or safe participation. 5. Refusal of regular hospital or outpatient visits, or consistently negative attitude, with no clearly scheduled next physician's appointment. 6. Currently participating in another interventional clinical trial of similar nature.

Design outcomes

Primary

MeasureTime frame
Completion rate of the 8-week telerehabilitation exercise program. A participant who completes the protocol-defined sessions within the prespecified allowance windows is considered a completer. Success criterion: completion rate 70% or higher (11/15 or more).

Secondary

MeasureTime frame
(i) Safety: incidence and severity of exercise-related adverse events (e.g., fracture, spinal cord compression, falls, injury, excessive fatigue, worsening pain). (ii) Protocol adherence: lesson attendance rate (out of 4), individual-session attendance rate (out of 3), self-directed exercise completion rate. (iii) Change from baseline at week 8 in: EQ-5D-5L (index/VAS), daily step count, longest continuous walking time, 5-STS time, PRO-CTCAE scores.

Contacts

Public ContactJunya Kinkawa

Rehab for JAPAN Inc.

kinkawa@rehabforjapan.com+81-50-5497-5155

Outcome results

None listed

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