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Study on the application of home exercise program for patients with multiple myeloma

Study on the application of home exercise program for patients with multiple myeloma

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069356
Enrollment
Unknown
Registered
2023-03-14
Start date
2023-03-15
Completion date
Unknown
Last updated
2023-06-04

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

Conditions

multiple myeloma

Interventions

Intervention Group:Routine care + Aerobic exercise
Control group:Routine care

Sponsors

The First Affiliated Hospital Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Clinical diagnosis of multiple myeloma, DS stage I-II (patients with hemoglobin >= 85 g/L, serum calcium <= 2.65 mmol/L, osteolytic lesions <= 3 on skeletal examination, and low serum or urine myeloma protein production); 2. Age 18-75 years; 3. ECOG score of 0 to 2; 4. Patients living with a partner or family member; 5. Good language expression and comprehension; 6. Knowing their condition and agreeing to participate in this study.

Exclusion criteria

Exclusion criteria: 1. Patients with motor, communication, or consciousness impairments; 2. Patients with spinal cord compression, unstable fractures, high risk of venous thrombosis, severe peripheral neuropathy and or other serious life-threatening conditions; 3. Patients with severe physical or psychological disorders that make cooperation impossible; 4. Patients with new onset of bone/back/neck pain; 5. Patients who live alone; 6. Those who do not agree to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
6-minute walk test, 6MWDT;

Secondary

MeasureTime frame
Quality of life, QOL;weary;pain;

Countries

China

Contacts

Public ContactMeiyun Zhang

The First Affiliated Hospital Zhejiang University School of Medicine

13857185837@163.com+86 138 5718 5837

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026