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Gender-Transformative Interventions and Normative Beliefs About Reproductive Decision-Making (Beyond)

27. července 2026 aktualizováno: Technical University of Munich

Beyond the Couple: Gender-Transformative Interventions and Normative Beliefs About Reproductive Decision-Making of Newly Married People in India

The ECOVI trial is a two-arm cluster randomized controlled trial (cRCT) conducted in rural and urban communities across Maharashtra, Andhra Pradesh, and Rajasthan, India, and funded by the European Research Council (ERC). The trial evaluates the impact of a couples-based financial literacy and gender-transformative intervention ("Let Us Grow Together: Economic Wellbeing for Families") on economic intimate partner violence (IPV), economic decision-making, and economic empowerment among 2,276 married couples across 150 clusters.

This sub-study examines an understudied downstream question: whether such couples-based programs change normative beliefs that extend beyond the treated couple's own relationship to younger generations, particularly their daughters and their sons. Specifically, we ask whether the intervention shifts how treated women and men think about who should have the main say in reproductive decisions for newly married couples, for their daughters and their sons. In an additional analysis, we examine whether respondents apply different standards when reproductive decisions concern their daughter and her husband versus their son and his wife. A difference in the endorsement of women's reproductive autonomy across the two scenarios may indicate an asymmetry in the application of egalitarian norms, whereby respondents are more accepting of autonomy for biological daughters than for daughters-in-law. We further examine whether the intervention reduces this gap by promoting more consistent endorsement of women's reproductive decision-making autonomy across both scenarios.

Items measuring normative beliefs regarding younger generations are added to the ECOVI endline survey before the start of endline data collection. This pre-registration protocol is submitted before any endline data is collected, providing a fully prospective analysis plan. All mediator variables, internalized gender norms, and female household decision-making participation are collected at both baseline and endline as part of the main ECOVI trial.

The sub-study pursues four interconnected objectives: (1) to estimate the causal effect of the intervention on normative beliefs regarding reproductive decision-making; (2) to test whether any such effect operates through a shift in internalized gender norms (the norm internalization channel); (3) to test whether any such effect operates through a shift in perceived community gender norms (the perceived norms channel); and (4) to test whether any such effect operates through an increase in women's participation in household decision-making (the agency channel).

Přehled studie

Typ studie

Intervenční

Zápis (Odhadovaný)

2276

Fáze

  • Nelze použít

Kontakty a umístění

Tato část poskytuje kontaktní údaje pro ty, kteří studii provádějí, a informace o tom, kde se tato studie provádí.

Studijní místa

      • Pune, Indie
        • Maharashtra; Rajasthan; Andhra Pradesh

Kritéria účasti

Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.

Kritéria způsobilosti

Věk způsobilý ke studiu

  • Dospělý

Přijímá zdravé dobrovolníky

Ano

Popis

Inclusion Criteria:

  • married and co-habiting husband-wife pairs;
  • women aged 18-49 and men aged 18 and older;
  • primary residence in a study cluster in Maharashtra, Andhra Pradesh, or Rajasthan;
  • completion of at least primary schooling (4th grade);
  • both partners provide written informed consent and agree to participate in six sessions, baseline and endline surveys, and SMS follow-ups;
  • both partners understand the local language used in sessions;
  • no plans for relocation or prolonged absence before endline.

Exclusion Criteria:

  • either partner under 18 years;
  • refusal of consent or unwillingness to participate by either partner;
  • serious physical or mental condition preventing safe active participation.

Studijní plán

Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.

Jak je studie koncipována?

Detaily designu

  • Primární účel: Prevence
  • Přidělení: Randomizované
  • Intervenční model: Paralelní přiřazení
  • Maskování: Žádné (otevřený štítek)

Zbraně a zásahy

Skupina účastníků / Arm
Intervence / Léčba
Experimentální: Let Us Grow Together: Economic Wellbeing for Families
The ECOVI intervention "Let Us Grow Together: Economic Wellbeing for Families" integrates financial literacy education with gender-transformative content on equitable household roles, communication skills, and joint decision-making, delivered in six structured community-based sessions for couples. Married couples in clusters assigned to the intervention receive a structured program of six community-based sessions. Each session lasts between 2.5 and 3 hours and includes participatory activities, discussions, and exercises. All six sessions would be conducted by the same two facilitators - one male and one female. The content integrates financial literacy (e.g., household budgeting, saving practices, joint financial planning) with gender-transformative training (e.g., equitable household roles, communication skills, conflict resolution, and fostering empathy between spouses). Sessions are delivered by trained facilitators in a group setting with fifteen couples, approximately every 2-4
The ECOVI intervention "Let Us Grow Together: Economic Wellbeing for Families" integrates financial literacy education with gender-transformative content on equitable household roles, communication skills, and joint decision-making, delivered in six structured community-based sessions for couples.
Žádný zásah: Control
Married couples in clusters assigned to the control arm do not receive the special couples training during the study period. Participants in control group continue with standard activities and resources available in the community but without the structured sessions provided to the intervention arm. This control condition represents the status quo against which the added effect of the intervention can be measured. After the conclusion of the study, control clusters may be offered the intervention materials or sessions via the NGO partners in case investigators find overall positive treatment effects, ensuring ethical considerations are me

Co je měření studie?

Primární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Intergenerational Normative Beliefs Items
Časové okno: T2 = endline (~6 months after intervention, approx. 1.5 years after baseline))
Normative beliefs regarding reproductive decision-making are assessed using three hypothetical scenario-based items with identical wording and response options. Respondents indicate who should have the main say in deciding whether and when a newly married couple has children in three contexts: (1) a newly married couple in the community, (2) the respondent's daughter and her husband, and (3) the respondent's son and his wife. Response options include wife, joint decision by spouses, husband, other family members, other, and prefer not to say.
T2 = endline (~6 months after intervention, approx. 1.5 years after baseline))

Další výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Internalized Gender Norms:
Časové okno: T1 = baseline (prior to session 1); T2 = endline (~6 months after intervention, approx. 1.5 years after baseline))
Women's own gender norm attitudes are measured using five items assessing personal beliefs about gender roles: (1) boys should have more educational opportunities than girls; (2) a man should have the final word about decisions in his home; (3) a wife should eat after her husband and children; (4) daughters should have equal inheritance rights as sons; and (5) it would be a good idea to elect a woman as village leader. Responses use a five-point agree/disagree scale. Items 1-3 are coded 1 if the respondent agrees or strongly agrees (traditional response); items 4-5 are reverse-coded so that disagreeing is coded 1 (traditional response). The score is the mean of available items, ranging from 0 to 1, with higher values indicating more traditional gender attitudes. The mediating variable is the endline score, with baseline score included as a covariate.
T1 = baseline (prior to session 1); T2 = endline (~6 months after intervention, approx. 1.5 years after baseline))
Perceived Community Gender Norms:
Časové okno: T1 = baseline (prior to session 1); T2 = endline (~6 months after intervention, approx. 1.5 years after baseline))
Perceived norms are measured using the same five items, but respondents are asked to estimate how many out of ten community members would agree with each statement. Items 1-3 are summed directly; items 4-5 are subtracted (reversed), yielding an additive index where higher scores indicate more traditional perceived community norms. The mediating variable is the endline score, with baseline score included as a covariate.
T1 = baseline (prior to session 1); T2 = endline (~6 months after intervention, approx. 1.5 years after baseline))
Household Decision-Making Participation:
Časové okno: T1 = baseline (prior to session 1); T2 = endline (~6 months after intervention, approx. 1.5 years after baseline))
Women's decision-making power is assessed across seven domains: healthcare or medication for herself; number of children and timing; contraception and family planning; children's marriage, healthcare, education, and rearing; major household purchases; spending on food and groceries; and spending on her own clothing. Each item is scored 1 (sole decision) to 4 (someone else decides), with responses 92 (not applicable) and 98 (prefer not to say) treated as missing. The composite score is the mean across available items, with higher values indicating less decision-making power. For interpretability, the scale is reverse-coded in all analyses so that higher scores indicate greater participation. The mediating variable is the endline score, with baseline score included as a covariate.
T1 = baseline (prior to session 1); T2 = endline (~6 months after intervention, approx. 1.5 years after baseline))
Covariates
Časové okno: T1 = baseline (prior to session 1); T2 = endline (~6 months after intervention, approx. 1.5 years after baseline))
  • Respondent age
  • Respondent education
  • Respondent socioeconomic status
  • Household economic strain
  • Residential type (rural vs. urban)
  • Living arrangement (co-residing with in-laws vs. not)
  • State fixed effects (Maharashtra, Andhra Pradesh, Rajasthan)
T1 = baseline (prior to session 1); T2 = endline (~6 months after intervention, approx. 1.5 years after baseline))

Spolupracovníci a vyšetřovatelé

Zde najdete lidi a organizace zapojené do této studie.

Vyšetřovatelé

  • Vrchní vyšetřovatel: Janina I Steinert, Dr., Technical University of Munich

Publikace a užitečné odkazy

Osoba odpovědná za zadávání informací o studiu tyto publikace poskytuje dobrovolně. Mohou se týkat čehokoli, co souvisí se studiem.

Obecné publikace

Termíny studijních záznamů

Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.

Hlavní termíny studia

Začátek studia (Aktuální)

15. července 2025

Primární dokončení (Odhadovaný)

30. listopadu 2026

Dokončení studie (Odhadovaný)

30. listopadu 2026

Termíny zápisu do studia

První předloženo

9. července 2026

První předloženo, které splnilo kritéria kontroly kvality

27. července 2026

První zveřejněno (Aktuální)

29. července 2026

Aktualizace studijních záznamů

Poslední zveřejněná aktualizace (Aktuální)

29. července 2026

Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality

27. července 2026

Naposledy ověřeno

1. července 2026

Více informací

Termíny související s touto studií

Další identifikační čísla studie

  • 101115963

Plán pro data jednotlivých účastníků (IPD)

Plánujete sdílet data jednotlivých účastníků (IPD)?

NE

Popis plánu IPD

Individual participant data (IPD) will not be shared. However, fully anonymized datasets may be shared with project partners and qualified researchers working on related topics (e.g., gender norms and economic violence) for secondary analyses, including cross-country or pooled analyses, subject to data sharing agreements and ethical approvals.

Access Criteria:

Available on request upon approval by overall study PI Prof. Dr. Steinert

Informace o lécích a zařízeních, studijní dokumenty

Studuje lékový produkt regulovaný americkým FDA

Ne

Studuje produkt zařízení regulovaný americkým úřadem FDA

Ne

Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .

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