Breast cancer. Malignant neoplasm of breast
Conditions
Interventions
Intervention 1: Control group:. Intervention 2: Intervention group:. Intervention 3: Intervention group:.
Sponsors
Iran University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 18-65 years old Having an acceptable level of cognitive function as a score of 21 or higher based on the Mini Mental Status Examination (MMSE) Unilateral or bilateral mastectomy or lumpectomy surgery Minimum 1 month and maximum 2 years after surgery (based on having chemotherapy) Breast cancer diagnosis for the first time
Exclusion criteria
Exclusion criteria: Disease recurrence leading to hospitalization Acute conditions leading to person's inability to participate in intervention sessions Absence more than 2 sessions
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Occupational performance. Timepoint: Before the intervention and in weeks 4 and 16 (follow up). Method of measurement: Canadian Occupational Performance Measure(COPM).;Occupational satisfaction. Timepoint: Before the intervention and in weeks 4 and 16 (follow up). Method of measurement: Canadian Occupational Performance Measure(COPM).;Occupational wholeness. Timepoint: Before the intervention and in weeks 4 and 16 (follow up). Method of measurement: Occupational Wholeness Questionnaire(OWQ). | — |
Secondary
| Measure | Time frame |
|---|---|
| Joint range of motion. Timepoint: Before the intervention and in weeks 4 and 16 (follow up). Method of measurement: Goniometer.;Lymphedema. Timepoint: Before the intervention and in weeks 4 and 16 (follow up). Method of measurement: Volumeter.;Strength. Timepoint: Before the intervention and in weeks 4 and 16 (follow up). Method of measurement: Dynamometer.;Upper extremity and hand disability. Timepoint: Before the intervention and in weeks 4 and 16 (follow up). Method of measurement: Shortened Disabilities of the Arm, Shoulder and Hand Questionnaire(QDASH).;Health condition. Timepoint: Before the intervention and in weeks 4 and 16 (follow up). Method of measurement: Patient-Reported Outcomes Measurement Information System(PROMIS).;Quality Of Life. Timepoint: Before the intervention and in weeks 4 and 16 (follow up). Method of measurement: Functional Assessment of Cancer Therapy- Breast(FACT-B).;Doing, being, belonging and becoming concepts. Timepoint: Before the intervention and in weeks 4 and 16 (follow up). Method of measurement: Occupational Wholeness Questionnaire(OWQ). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Afsoon Hassani Mehraban
Iran University of Medical Sciences
Outcome results
None listed