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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01557686
Other study ID # H-4-2010-046 Pilot
Secondary ID
Status Completed
Phase Phase 0
First received March 15, 2012
Last updated March 16, 2012
Start date May 2010
Est. completion date February 2011

Study information

Verified date March 2012
Source Universitetshospitalernes Center for Sygepleje
Contact n/a
Is FDA regulated No
Health authority Denmark: The Danish National Committee on Biomedical Research Ethics
Study type Interventional

Clinical Trial Summary

The purpose of this pilot study is to test an exercise-based multidimensional intervention for patients with acute leukaemia undergoing consolidation chemotherapy in the context of outpatient management. Further, to test for safety, feasibility and preliminary effect on physical and functional capacity, and health related quality of life.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date February 2011
Est. primary completion date February 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients that are able to speak Danish > 18 years and newly diagnosed with acute leukæmia (MDS, AML, CMML, APL or ALL)

- Normal EKG, blood pressure and pulse

- Signed informed written consent

Exclusion Criteria:

- Medical reason that contraindicates physical activity

- Patients diagnosed with a symptomatic cardiac disease within the last three months.

- Documented bone metastasis

- Dementia, psychotic

- Cannot write or read Danish

- Patients unable to carry out baseline tests

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms


Intervention

Behavioral:
Health counseling and exercise
The intervention is initiated during chemotherapy treatment (consolidation) in the outpatient clinic and continues for 6 weeks. The intervention is a three hour/wk supervised in-hospital programme of aerobic (stationary cycle) and functional muscle training, progressive relaxation training, nutrition supplement (protein and carbohydrate) immediately after training and two health-promoting counseling sessions - Further, patients are fitted with a step counter pedometer.

Locations

Country Name City State
Denmark Copenhagen University Hospital Copenhagen
Denmark Herlev Hospital Herlev

Sponsors (3)

Lead Sponsor Collaborator
Universitetshospitalernes Center for Sygepleje Lundbeck Foundation, Novo Nordisk A/S

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Feasibility - adherence rates Percentage of intervention participation Adherence to the intervention components from baseline to 6 weeks Yes
Secondary Adverse events Number and type of adverse events baseline to 6 weeks Yes
Secondary 6MWD Change in distance in meter Change from baseline in 6MWD at 6 weeks Yes
Secondary Attrition Number of patients that withdrew from the project Withdrawal from the project from baseline to 6 weeks Yes
Secondary Timed chair stand Change in the number of repetitions Change from baseline in timed chair stand at 6 weeks Yes
Secondary Timed bicep curl Change in number of repetitions Change from baseline in timed bicep curl at 6 weeks Yes
Secondary FACT-Anemia Change in scores for quality of life/function Change from baseline in FACT-An at 6 weeks No
Secondary HADS Change in scores for emotional wellbeing Change from baseline in HADS at 6 weeks No
Secondary SF36 Change in scores for general health Change from baseline in SF36 at 6 weeks No
Secondary MDSAI Change in scores for symptom burden Change from baseline over time (1,2,3,4,5,6 weeks) No
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