Reproductive health program for young women

INTERVENTION: After conducting a preliminary, experimental investigation procedure, the program for promoting reproductive health based on the PAPM was applied step by step to the intervention group, and the program was replaced with educational material for the control group. The random allocation sequence was conducted with a 1:1 ratio using a computer‐generated program (https://www.randomizer.org/) after the pretest. The program is a tailored program whereby each stage of the PAPM (Stages 1, 2, and 3) is outlined, using components of the Information‐Motivation‐Behavioral skills model. The program comprises intervention strategies, such as lectures; periodic information and information tailored to individuals’ needs; small group discussions; question and answer sessions (Q&A); individual counselling; case experience using videos; and practical training. The total duration of the intervention is 8 weeks. Outcomes are measured at three timepoints: T0 indicates the baseline, T1 indicates 1 week after the seminar (2 weeks after baseline) and T2 indicates within 1 week after completion of the interventions (8 weeks after baseline). CONDITION: Reproductive health ; Pregnancy and Childbirth PRIMARY OUTCOME: ; 1. Reproductive health‐promoting behavior measured using self‐reported questionnaire via online survey at T0 (baseline), T1(2 weeks after baseline), and T3 (after completion of intervention/8 weeks after baseline); 2. Rate of contraception use measured using self‐reported questionnaire via online survey at T0, T3; ; Outcomes are measured at three timepoints: T0 indicates the baseline, T1 indicates 1 week after the seminar (2 weeks after baseline) and T2 indicates within 1 week after completion of the interventions (8 weeks after baseline).; SECONDARY OUTCOME: ; 1. Reproductive health knowledge measured using self‐reported questionnaire via online survey at T0, T1, T3; 2. Reproductive health belief measured using self‐reported questionnaire via online survey at T0, T1, T3; 3. Reproductive health motivation measured using self‐reported questionnaire via online survey at T0, T1, T3; 4. Reproductive health self‐efficacy measured using self‐reported questionnaire via online survey at T0, T1, T3; ; Outcomes are measured at three timepoints: T0 indicates the baseline, T1 indicates 1 week after the seminar (2 weeks after baseline) and T2 indicates within 1 week after completion of the interventions (8 weeks after baseline).; INCLUSION CRITERIA: 1. Young adult women aged between 18 and 25 2. Women who had coitus in the last 3 months and had partners Phase 2 of the study: 3. Women in Stages 1, 2, and 3 of the PAPM for reproductive health via an online survey