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Clinical Trials/NCT04617145
NCT04617145
Completed
Not Applicable

Impact of Aerobic Versus Resistive Training on Functional Capacity in Acute Myeloid Leukemia Survivors; a Comparative Study

Cairo University1 site in 1 country60 target enrollmentApril 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Acute Myeloid Leukemia in Remission
Sponsor
Cairo University
Enrollment
60
Locations
1
Primary Endpoint
Six minutes walking Distance
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

Sixty patients with AML from both sexes aged from 35-45 years were selected from hematology department in Nasser Institute Hospital where the study was conducted. Patients were randomly assigned into two groups equal in number. Group (A) underwent aerobic exercises in the form of cycling with 50-60% of maximum heart rate. Group (B) underwent resistive training conducted in the form of a series of exercises using free weights, and dumbles. Sessions were conducted three times /week for eight weeks. Six minutes' walk test (6MWT), 10 repetitions maximum test (10 RM), ventilatory function test, fatigue and quality of life (QOL) scales were used to assess functional capacity in both groups.

Detailed Description

Aerobic Ex Group: Included 30 patients who underwent aerobic training with 50 %-60% of maximum heart rate in the form of cycling by Bicycle ergometer for eight weeks, three sessions/week. Resistive Ex Group: Included 30 patients who underwent a resistive training which were conducted in the form of a series of exercises using free weights, and dumbles to increase the strength of arms, pectoral muscles, abdominal, back muscles and gluteal region. Patients carried out three sets of 20-30 dynamic repetitions or static isometric exercises for 40-60 seconds for each muscle group and rested 1-2 min between series. Sessions were conducted three sessions/week for eight weeks.

Registry
clinicaltrials.gov
Start Date
April 1, 2018
End Date
October 1, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Heba Ahmed Ali Abdeen

Assistant Professor

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Acute myeloid leukemia survivors from both sexes
  • Their age ranged from 35-45 years.
  • Patients were in remission stage contains less than 5% blast cells in their bone marrow, absolute neutrophil count (\>1000/microL), platelet count(\>100,000/microL),and independence from red cell transfusion.

Exclusion Criteria

  • Extramedullary leukemia
  • musculoskeletal deformities
  • severe anemia (hemoglobin less than 8g/dl).
  • Autoimmune thrombocytopenia (platelets less than 10000UL or leucocytes count more than 3000UL).

Outcomes

Primary Outcomes

Six minutes walking Distance

Time Frame: It is performed before and after the study(8 weeks interval) for both groups

which used to measure the distance the patient was able to walk over a total of six minutes According to American thorax society guidelines; patients were instructed to walk as fast as long as possible , in a 30 meters obstacle free corridor limited by turnaround cones and distance was calculated

10 repetition maximum test

Time Frame: It is performed before and after the study(8 weeks interval) for both groups

which the greatest amount of weight a person can lift number of times. The amount of weight that can be lifted exactly 10 times is 10 RM

Vital capacity

Time Frame: It is performed before and after the study(8 weeks interval) for both groups

was measured by using electronic spirometry used to conduct ventilatory function testing

Secondary Outcomes

  • Maximum oxygen consumption(It is performed before and after the study(8 weeks interval) for both groups)
  • Fatigue assessment scale (FAS)(It is performed before and after the study(8 weeks interval) for both groups)
  • Quality of life questionnaire (QOL)(It is performed before and after the study(8 weeks interval) for both groups)

Study Sites (1)

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