Impact of educational pain management program on pain intensity and quality of life in cancer patients

Effect of a designed pain management program education on pain and quality of life of cancer patient with moderate to severe pain in chemotherapy and radiotherapy units in Nemazee hospital _ Shiraz 1389

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT201110012812N3

Enrollment

Registered

2011-12-30

Start date

2010-09-23

Completion date

Unknown

Last updated

2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cancer. Malignant neoplasms

Interventions

Intervention 1: control group: patients in this group received routine clinical care.they complete The BPI questionnaire at the first interview, 2, 4 and 8 weeks after intervention and EORCT QLQ - C3

Behavior

control group: patients in this group received routine clinical care.they complete The BPI questionnaire at the first interview, 2, 4 and 8 weeks after intervention and EORCT QLQ - C30 questionnaire

experimental group:patients in this group compelet BPI and EORCT questionnaires. then recived education that consists of 6 session educational pain management in 20-30 minute during 6 week to addition

Eligibility

Sex/Gender

All

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: inclusion criteria were patients:1) diagnosed with cancer,2) treatment with chemo and radiotherapy 3) experiencing pain (4 & >4) related to cancer with doctor diagnosed 4) over the age of 18 years old 5)able to read and write persian. Patients with pain related to treatment with doctor diagnosed , participant in other educational pain management program and with a history of cognitive, psychatric disorder were excluded this study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pain intensity. Timepoint: befor intervetion, 2, 4 , 8 weeks after intervetion. Method of measurement: breif pain inventory.;Quality of life. Timepoint: befor intervetion, 4 , 8 weeks after intervetion. Method of measurement: EORCT QLQ - C30 qestionnaire.	—

Secondary

Measure	Time frame
Pain satisfaction. Timepoint: befor intervetion, 2, 4 , 8 weeks after intervetion. Method of measurement: breif pain inverntory.;Interfrence with daily function. Timepoint: befor intervetion, 2, 4 , 8 weeks after intervetion. Method of measurement: breif pain inventory.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Farkhondeh Sharif

Shiraz University of Medical Sciense

fsharif@sums.ac.ir+98 71 1626 6931

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026