The effect of consultative-supportive plan on perceived stress, hope and sleep quality
Not Applicable
Recruiting
- Conditions
- Breast.Malignant neoplasm of breast
- Registration Number
- IRCT20180618040128N1
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
Age over 18 years
Ability to read and write in Persian
Having access to phone
Suspected of breast cancer and having a mass requiring biopsy
Exclusion Criteria
Cancellation of participation in the study
Taking sedatives, antidepressants or anti-anxiety
History of cancer and chronic diseases
Major stressful events in the past six months (death of first class relatives, severe family members, financial failures, accidents, severe family disputes with the spouse)
Disability (mental, hearing, vision and speech) or mental illness
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Perceived stress. Timepoint: Before the intervention, before receiving the biopsy result and two weeks after receiving the biopsy result. Method of measurement: Cohen Perceived Stress Questionnaire.;Hope. Timepoint: Before the intervention, before receiving the biopsy result and two weeks after receiving the biopsy result. Method of measurement: Snyder's hope Questionnaire.;Sleep quality. Timepoint: Before the intervention, before receiving the biopsy result and two weeks after receiving the biopsy result. Method of measurement: Petersburg's Sleep Quality Scale.
- Secondary Outcome Measures
Name Time Method