The impact of training to do pap smear for early dignosis of cervical cancer

Evaluate the effect of training Health Belief model-based education through online mobile messaging application on Bushehrian women's beliefs and performances related to Pap smear experiment

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2016062928702N1

Enrollment

106

Registered

2016-08-13

Start date

2016-08-22

Completion date

Unknown

Last updated

2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervical Cancer. Malignant Neoplasm of Cervix uteri

Interventions

Intervention 1: The participants of intervention group receives health belief model-based training content within one month through telegram messenger application. Intervention 2: The control group do

Prevention

The participants of intervention group receives health belief model-based training content within one month through telegram messenger application.

The control group doesn't receive any training.

Eligibility

Sex/Gender

Female

Age

20 Years to 50 Years

Inclusion criteria

Inclusion criteria: inclusion criteria: literacy; having a smart phone and telegram messaging application; passing at least six months of marriage, lack of/not doing of Pap smear in past three years. Exclusion criteria: unwillingness to participate in the study, presence of cervical cancer or other cancers in the genital tract, presence of hysterectomy history.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Doing Pap SmearTest. Timepoint: Before and after three months of training. Method of measurement: Questionnaire.	—

Secondary

Measure	Time frame
Knowledge of Cervical Cancer. Timepoint: Before, immediately and after three months training. Method of measurement: Questionnaire.;Perceived Susceptibility. Timepoint: Before, immediately and after three months training. Method of measurement: Questionnaire.;Perceived Severity. Timepoint: Before, immediately and after three months training. Method of measurement: Questionnaire.;Perceived Benefits. Timepoint: Before, immediately and after three months training. Method of measurement: Questionnaire.;Perceived Barriers. Timepoint: Before, immediately and after three months training. Method of measurement: Questionnaire.;Health Motivation. Timepoint: Before, immediately and after three months training. Method of measurement: Questionnaire.	—

Measure

Time frame

Knowledge of Cervical Cancer. Timepoint: Before, immediately and after three months training. Method of measurement: Questionnaire.;Perceived Susceptibility. Timepoint: Before, immediately and after three months training. Method of measurement: Questionnaire.;Perceived Severity. Timepoint: Before, immediately and after three months training. Method of measurement: Questionnaire.;Perceived Benefits. Timepoint: Before, immediately and after three months training. Method of measurement: Questionnaire.;Perceived Barriers. Timepoint: Before, immediately and after three months training. Method of measurement: Questionnaire.;Health Motivation. Timepoint: Before, immediately and after three months training. Method of measurement: Questionnaire.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzita Noroozi

Bushehr University of Medical Sciences, Salman Farsi St, Bahmani, Bushehr, Iran

azitanoroozi@yahoo.com+98 77 3332 2081

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026