The aim of this trial is to assess the effectiveness of joint provision of community group-based demonstration counseling methods with routine individual family planning counseling provided to prenatal and postnatal women on postpartum contraception acceptance in the West Shoa Zone, Oromia, Ethiopia. A two-arm cluster randomized control trial will be conducted to compare the routine individual facility-based family planning counseling with the joint provision of individual and community group-based counseling with a process of arranged demonstration on the later part. The study will be conducted from March 1, 2025, to May 30, 2026. A sample of 598 women (21 women per 28 clusters) will be selected by a two-stage (stratification and clustering) sampling. A structured questionnaire will be used to collect the data. The data will be entered into STATA (V16). A goodness of fit test using Pearson's chi-square and a multicollinearity test will be checked. Multinomial logistic regression will be used for analysis. The main questions it aims to answer are: 1. Will postpartum women in the intervention group (joint provision of individual and community group-based counseling) be more likely to use contraception? 1. Percent of postnatal women who receive any method from the intervention group. 2. Percent of postnatal women who receive any method from the control group. 2. Will postpartum women in the intervention group, subject to an intervention group, prefer highly effective contraceptive methods? 1. Percent of postnatal women who receive highly effective methods from the intervention group. 2. Percent of postnatal women who receive low-effective methods from the control group. 3. Percent of postnatal women who receive highly effective methods from the control group. 4. Percent of postnatal women who receive low-effective methods from the intervention group.
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Magnitude (percentage) of postnatal women who use any contraceptive method; 2. The percentage of each contraceptive method (choices) utilized by postnatal women
Timeframe: Recruitment to end of the study: 1 year