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Effectiveness of Complementary Medicine in Improving pain and fatigue in Leukemia Patients

Not Applicable
Conditions
eukemia.
Acute lymphoblastic leukemia [ALL]
C91.0
Registration Number
IRCT20150302021307N3
Lead Sponsor
Ahvaz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
107
Inclusion Criteria

Eighteen years or older
Undergoing chemotherapy
At least 3 months after diagnosis of acute leukemia

Exclusion Criteria

Known disorders of pain in their medical history
Underlying co-morbidities such as diabetes or other types of cancer

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain and fatigue intensities more than 3 according to the 0 to 10 numeric rating scale. Timepoint: Pain and fatigue intensities will be measured before intervention. During the four weeks of interventions, pain and fatigue intensities will be measured at the end of each week of study. Also, one week and two weeks after end of the interventions (week 5 and week 6), the pain and fatigue intensities will be measured again. Totally, pain and fatigue intensities will be measured for 7 times. Method of measurement: 0-10 Numeric Rating Scale.
Secondary Outcome Measures
NameTimeMethod
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