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Strength Training and ADLs in Childhood Leukemia and Lymphoma Patients

T

Technical University of Munich

Status

Completed

Conditions

Childhood Cancer

Treatments

Other: Exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT03934060
DJCLS 15 R/2016

Details and patient eligibility

About

Reduced activity levels and reduced muscular strength could severely impair the activities of daily living (ADLs) in pediatric leukemia and Non-Hodgkin lymphoma patients. Increased muscle strength is associated with improved accomplishment of ADLs and consequently greatest possible normality, autonomy and mobility. Primary outcome of this RCT (n=20/20) is the analysis of effects of a treatment-associated and close to every day life strength training (2-3 times/week) compared to a general exercise program (standard care).

Enrollment

40 patients

Sex

All

Ages

4 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosed with Acute Leukemia or Non-Hodgkin Lymphoma
  • Diagnosed and/or treated at the Kinderklinik München Schwabing, Technische Universität München
  • Informed consent as documented by signature

Exclusion criteria

  • Medical contraindications regarding strength training (e.g. risk of bleeding, ...)
  • Contraindications to one of the inclusion criteria mentioned above
  • Inability to follow the procedures and understand the intervention and assessments of this study, e.g. due to cognitive impairment, language problems, psychological disorders etc.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

Intervention
Experimental group
Description:
Supervised exercise training including specific strength training tools and general exercise contents (standard care), 2-3 times per week, 30 minutes per session
Treatment:
Other: Exercise
Control
No Intervention group
Description:
Supervised exercise training regarding general exercise contents (standard care), 2-3 times per week, 30 min per session

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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