Patients with breast cancer who suffer from pain.
Conditions
Interventions
Intervention 1: Intervention group1: They will receive group training on the designed pain management program through 6 120-minute sessions. This intervention includes the introduction of the group an
Sponsors
The University of Isfahan
Eligibility
Sex/Gender
Female
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: Breast cancer diagnosis Receive chemotherapy experience pain Agreeing to participate in the research
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain experienced. Timepoint: Before intervention, immediately after intervention, 1 month after intervention. Method of measurement: Brief pain intensity questionnaire (Klind, 1991). | — |
Secondary
| Measure | Time frame |
|---|---|
| Life expectancy. Timepoint: Before intervention, immediately after intervention, 1 month after intervention. Method of measurement: Life expectancy questionnaire of Snyder, Harris and Anderson (1991). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMohsen Arefian
The University of Isfahan
Outcome results
None listed