Condition 1: cervical cancer. Condition 2: consulting. Condition 3: drug addiction. Malignant neoplasm of cervix uteri Counselling, unspecified Mental and behavioural disorders due to multiple drug use and use of other psychoactive substances
Conditions
Interventions
Intervention 1: Intervention group: The objectives of this study will be described by researcher at a session to the participants courteously and friendly. The meeting time will be 45 until 60 minutes
Early detection
Intervention group: The objectives of this study will be described by researcher at a session to the participants courteously and friendly. The meeting time will be 45 until 60 minutes. Explaining the
Control group: Members of the control group will be selected in accordance with inclusion criteria. They will receive the questionnaire without any training.
Behavior of both groups will be assessed
Sponsors
Vice Chancellor for research of Hamadan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
20 Years to 100 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: The inclusion criteria for eligibility into the study are as follows, passing at least 3 years after the first sexual intercourse or married women above 21 years; not having had Pap test in the past three years; not to suffer cervical cancer and to consume Methadone. Also the participants will be studied with their consent. Exclusion criteria: Exclusion criteria are unwillingness of the community members to continue participating in the study and formal training by other organizations during the study.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pap smear and cervical cancer awareness. Timepoint: Before the intervention, immediately after the intervention, one to two months after the intervention. Method of measurement: Researcher made questionnaire.;Self efficacy. Timepoint: Before the intervention, immediately after the intervention, one to two months after the intervention. Method of measurement: Researcher made questionnaire.;Function. Timepoint: Before the intervention, one to two months after the intervention. Method of measurement: Observed test papers.;Response Efficacy. Timepoint: Before the intervention, immediately after the intervention, one to two months after the intervention. Method of measurement: Researcher made questionnaire.;Vulnerability Perceived. Timepoint: Before the intervention, immediately after the intervention, one to two months after the intervention. Method of measurement: Researcher made questionnaire.;Perceived severity. Timepoint: Before the intervention, immediately after the intervention, one to two months after the intervention. Method of measurement: Researcher made questionnaire.;Response costs. Timepoint: Before the intervention, immediately after the intervention, one to two months after the intervention. Method of measurement: Researcher made questionnaire.;Motivation. Timepoint: Before the intervention, immediately after the intervention, one to two months after the intervention. Method of measurement: Researcher made questionnaire.;Fear. Timepoint: Before the intervention, immediately after the intervention, one to two months after the intervention. Method of measurement: Researcher made questionnaire.;Perceived rewards. Timepoint: Before the intervention, immediately after the intervention, one to two months after the intervention. Method of measurement: Researcher made questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| -. Timepoint: -. Method of measurement: -. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactElham Fakouri
Nursing & Midwifery Faculty; Hamadan University of Medical Sciences.
Outcome results
None listed