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Cognitive Function After Stem Cell Transplantation

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Charité University Medicine Berlin

Status and phase

Unknown
Phase 3

Conditions

Stem Cell Transplantation
Cognitive Impairment
Fatigue

Treatments

Other: Endurance exercise
Other: Counseling

Study type

Interventional

Funder types

Other

Identifiers

NCT00884338
EA4/028/09

Details and patient eligibility

About

The trial will evaluate the effects of an exercise program on the physical and cognitive performance of patients with hematological neoplastic diseases after high dose chemotherapy with stem cell support.

Full description

Patients (n = 60) will be randomized to an exercise or a control group. The randomization will be stratified for allogeneic or autologous blood stem cell transplantation. Patients in the exercise group will carry out an endurance training consisting of walking on a treadmill at a speed corresponding to 80% of the maximum heart rate. The exercise program will be carried out 3 times weekly for 8 weeks. Patients in the control group will receive counseling about exercise and behavioural techniques to reduce fatigue, but they will not participate at a structured exercise program. Physical performance (VO2max), cognitive function, mood and quality of life will be evaluated at recruitment and after 8 weeks.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18 - 70
  • Hematological neoplastic disease
  • Treatment with high-dose chemotherapy with peripheral blood stem cell transplantation in the previous 3 years
  • Karnofsky-Index > 80%
  • Ability to understand German

Exclusion criteria

  • Cardiorespiratory, metabolic, inflammatory or osteoarticular diseases which can be aggravated by exercise
  • Psychosis
  • Organic brain damage
  • Dementia
  • PBSCT in the previous 6 weeks
  • Pathological stress test at admission

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

Exercise
Experimental group
Treatment:
Other: Endurance exercise
Control group
Active Comparator group
Treatment:
Other: Counseling

Trial contacts and locations

1

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Central trial contact

Fernando Dimeo, MD

Data sourced from clinicaltrials.gov

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