lymphoma. Small cell B-cell lymphoma, unspecified site
Conditions
Interventions
Intervention 1: The first intervention group: At first, in the first session of his intervention, the researcher appeared in the department one hour before the start of chemotherapy, then after obtain
Sponsors
Semnan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Being aged between 18 to 60 years A definitive diagnosis of lymph node cancer and its type (Hodgkin's and non-Hodgkin's) has been made by a hematologist and oncologist. Receiving ABVD drug regimen in Hodgkin's lymphoma patients Receiving drug regimen R-CHOP or R-EPOCH in non-Hodgkin's lymphoma patients Being alert and trainable No mental disorders Not using muscle relaxants, sleeping pills and psychoactive drugs Interested in both music therapy and progressive muscle relaxation Absence of physical disorders such as (hearing and movement problems) and acute mental disorders At least 3 months have passed since the person was diagnosed with cancer Having a normal body mass index Having hemoglobin of at least 8gr/dl
Exclusion criteria
Exclusion criteria: Refusal to continue participating in the study Decreased level of alertness while studying The occurrence of severe physical complications caused by the disease Metastasis to other parts of the body Implementation of less than four days a week and its non-compliance with the training given death of the patient suffering from diseases characterized by fatigue (multiple sclerosis, fibromyalgia, AIDS, joint rheumatism)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Level of quality of life. Timepoint: Before the start of the intervention, it will be completed at the end of the first and fourth week after the start of the intervention. Method of measurement: The score given by the patient from the questionnaire (EORTC QLQ-C30) which is specific for cancer patients and measures 5 functional domains, 9 symptom domains and one general domain of quality of life. This questionnaire is based on a four-point Likert scale. Not at all (score 1), a little (score 2), a bit (score 3), very much (score 4). To calculate the score of each subscale, the score of each item related to that subscale is added together. To calculate the total score of the questionnaire, the scores of all questionnaire items are added together. The minimum and maximum score of this questionnaire is 30 and 126. The higher the score obtained from this questionnaire, the higher the quality of life and vice versa.;Fatigue intensity. Timepoint: Before the start of the intervention, it will be completed at the end of the first and fourth week after the start of the intervention. Method of measurement: The questionnaire (MFI) consists of 20 items and 5 subscales of general fatigue (4 questions), physical fatigue (4 questions), decreased activity (4 questions), decreased motivation (4 questions) and mental fatigue (4 questions), which It is used to measure fatigue. The scoring of the questionnaire is on a 5-option Likert scale from 1 = yes, completely true to 5 = no, completely false. Questions number 2, 5, 9, 10, 13, 14, 16, 17, 18, 19 are graded in reverse order and are graded as 5 completely correct to 1 completely incorrect. To get the overall score of the questionnaire, the scores of all items are added together. The total score of each field is 4-20 and the total score of fatigue determined by the sum of the scores of the fields can be between 20-100. A higher score indicates greater fatigue. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSajad Salehipour
Semnan University of Medical Sciences
Outcome results
None listed