Quality of life. Other stressful life events affecting family and household
Conditions
Interventions
Intervention 1: Intervention group: Individual supportive counseling will be provided by the researcher (a master's student in midwifery counseling) for 30-45 minutes per session. Counseling sessions
Sponsors
Babol University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 54 Years
Inclusion criteria
Inclusion criteria: Diagnosis of high-risk human papillomavirus infection by specialized tests (PCR) Women who have been diagnosed with human papillomavirus for at least 3 months (due to the impact of a positive result on study outcomes, including quality of life and general health) Women who have been diagnosed with high-risk human papillomavirus for a maximum of two years. Age 18-54 years Willingness to participate in the study with informed consent Having at least literacy and access to a mobile phone
Exclusion criteria
Exclusion criteria: Cervical cancer and other cancers in the studies conducted Known mental disorders Taking psychotropic, anti-anxiety, antidepressant History of disease-related counseling in the past 6 months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Quality of life of women infected with human papillomavirus. Timepoint: They will complete a quality of life questionnaire before the start of the study, six weeks, and four months after the start of the study. Method of measurement: Quality of life questionnaire for people with human papillomavirus. | — |
Secondary
| Measure | Time frame |
|---|---|
| General health. Timepoint: They will complete a general health questionnaire before the start of the study, six weeks, and four months after the start of the study. Method of measurement: Goldberg 12-question general health questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFereshteh Behmanesh
Babol University of Medical Sciences
Outcome results
None listed