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Impact of Various Exercise Regimens on Physical Function and Quality of Life in Patients with Hematologic Malignancies

Impact of Various Exercise Regimens on Physical Function and Quality of Life in Patients with Hematologic Malignancies

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124599
Enrollment
Unknown
Registered
2026-05-14
Start date
2026-05-25
Completion date
Unknown
Last updated
2026-05-18

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

Conditions

Hematologic Malignancies

Interventions

control group:Daily Activity Education
Intervention Group:Exercise Therapy

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Study participants diagnosed with hematologic malignancies (confirmed by imaging studies, hematologic tests, and pathologic examination) 2. Aged 18–80 years (inclusive) 3. Capable of performing independent light- to moderate-intensity exercise 4. No severe cardiopulmonary dysfunction or other contraindications to exercise 5. No implanted cardiac pacemakers or other metal devices 6. No cognitive impairment and able to complete assessment scales 7. Voluntary participation with signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Untreated unstable bone lesions (especially pathological fractures and spinal cord compression) that cannot tolerate physical stress during exercise (highly increased fracture risk in these areas). 2. Severe cardiopulmonary diseases: Recent (within 6 months) myocardial infarction, stroke, or other major cardiovascular events (unstable angina, aortic stenosis, aortic aneurysm, decompensated heart failure, uncontrolled arrhythmias, chest pain, dyspnea, third-degree heart block). 3. Acute critical illnesses, including acute systemic diseases with deterioration, acute myocardial infarction, acute infections and endocarditis, acute deep vein thrombosis. 4. Presence of severe infections, anemia (hemoglobin <30 g/L), or thrombocytopenia (platelets <10×10^9/L). 5. Severe cognitive impairment or psychiatric disorders that prevent cooperation with scale assessments and exercise therapy. 6. Expected survival <12 months. 7. Current participation in other clinical trials or interventional studies. 8. Concurrent malignancies.

Design outcomes

Primary

MeasureTime frame
(Multidimensional Fatigute Inventory,MFI)-20;Self-Rating Anxiety ScaleSelf-Rating Depression Scale;(EORTC QLQ-C30);(Timed Up and Go Assessment of Biomechanical Strategies,TUG-ABS);Six Minute Walk Test;(skeletal muscle mass,SMM);(30-Second Chair Stand);Grip strength;Calf circumference;

Secondary

MeasureTime frame
Eastern Cooperative Oncology Group;(Barthel Index of ADL);

Countries

China

Contacts

Public ContactXiang Jie

Affiliated Hospital of Xuzhou Medical University

Xj1111@163.com+86 137 7597 0412

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 22, 2026