cancer. Anxiety disorder due to known physiological condition
Conditions
Interventions
Intervention 1: Intervention group: Intervention group: Before the chemotherapy administration, participants will be given the questionnaire to filled in order to assess their anxiety. Then, each part
Sponsors
University of Baghdad
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: All adult patients who have been diagnosed with cancer and admitted to hospitals to receive chemotherapy will be included in the study. Adult patients above 18
Exclusion criteria
Exclusion criteria: Patients with lower than sixth-grade educational levelPatients who do not know their medical diagnosis Patients who have mental illnesses, Patients who are blind or deaf, Patients who are undergoing radiotherapy Furthermore, subjects will be excluded if they could not complete the session of spiritual or music therapy before the administration of chemotherapy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome variable is the level of chemotherapy-induced anxiety that can be changed based on Quran or music. Timepoint: before intervention and 30 minutes after intervention. Method of measurement: The Arabic version of State-Anxiety Inventory (STAI) will be used to assess the level of chemotherapy-induced anxiety. | — |
Countries
Iraq
Contacts
Public ContactMohammed Baqer Al-Jubouri
University of Baghdad
Outcome results
None listed