Implementation Science and Impact Evaluation of PfR Programme: A Hybrid cRCT Design

NCT ID: NCT05105373

Last Updated: 2023-12-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

3162 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-08-06

Study Completion Date

2022-12-30

Brief Summary

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The Implementation science and impact evaluation of PfR programme: A hybrid cRCT design study will use an effectiveness-implementation hybrid type 2 design to a) determine the effectiveness and cost-effectiveness of PfR, and b) determine the feasibility and impact of three different implementation strategies in terms of programme delivery. A cluster randomised controlled trial (cRCT) will examine the effectiveness, cost-effectiveness, and implementation of the Parenting for Respectability (PfR) programme on the reduction of violence against children and gender based violence in comparison to those receiving an hour lecture on parenting in the Wakiso and Amuru districts of Uganda (N = 54 clusters, 2,160 parents, 1,080 children, 1:1 allocation ratio).

Detailed Description

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Intimate partner violence (IPV) and violence against children (VAC) are interlinked and are major social, development and public health concerns. Globally it is estimated that approximately 30% ever-partnered women worldwide have experienced physical and/or sexual violence by an intimate partner at some point in their lives. IPV prevalence among women in Uganda is very high. The Uganda Demographic and Health Survey 2018 found that 36% of women had ever experienced partner physical violence, while 22% had ever experienced partner sexual violence. Violence against children is extremely widespread globally, with approximately half of all children - one billion aged 2-17 years - reporting having experienced violence in the past year. Furthermore, one in five women and up to one in ten men have been victims of sexual violence in childhood. The Uganda national VAC survey 2015 found that 59% girls and 68% boys had experienced physical violence in their childhood, and 35% girls and 17% boys had experienced sexual violence in their childhood. Such violence in Uganda and most Sub-Saharan African countries is usually perpetrated by people known to children in their homes and community. IPV and VAC are major causes of morbidity and mortality, they undermine the social functioning of the victims and their families, and have lifetime consequences for physical, sexual, reproductive and mental health. The prevention of both forms of violence would contribute to many Sustainable Development Goals since they strain health systems, lower educational achievement and economic productivity, and undermine economic and social development, and elimination of IPV is essential to Goal Five.

Many studies confirm the link between VAC and IPV, suggesting the need for an integrated approach to their prevention. A recent narrative review identified six ways in which they are interrelated: they have many shared risk factors, starting in the family; social norms legitimise both and discourage children and women from seeking help; both often occur within the same household both can be transmitted across generations; they can have similar consequences across the lifespan, and finally, both intersect in adolescence, a time of heightened vulnerability to violence.

Factors perpetuating IPV and VAC exist at multiple socio-ecological levels. For IPV, familial level factors include having been abused as a child, having an absent or rejecting father, inter-partner conflict, and male control of wealth and decision-making. Community level factors include women's isolation and male peer groups that legitimize men's violence. At the macro level IPV is associated with cultural norms that condone violence within the family, schools and community, establish rigid gender roles and link masculinity to toughness, male honour, dominance and ownership of women, and it thrives where policy, legislation and implementation of laws is weak. VAC is more likely in families that have difficulties developing stable, warm and positive relationships, where parents are unresponsive to their children, have harsh or inconsistent parenting styles, believe that corporal punishment is an acceptable form of discipline or have a poor understanding of child development, and therefore unrealistic expectations about the child's behaviour.

Recognizing that IPV is perpetuated at multiple levels, preventative interventions often focus on other psychosocial problems, e.g. poverty or alcohol abuse, as well as on inter-partner violence, although they are more effective if their main aim is to reduce IPV. The shared familial risk factors for IPV and VAC, and the increasing policy interest in optimizing parenting influence, provides a great opportunity for early intervention. An increasing number of parenting programs are being implemented and tested in LMICs to reduce VAC, and evidence is emerging that, if delivered by trained lay workers, they can be effective in improving child outcomes. However, interventions directly addressing early prevention of both IPV and VAC in LMICS remain limited.

Furthermore, very few parenting programs in LMICs harness cultural drivers and pre-existing motivations to change behaviour. In sub-Saharan Africa little attention has been paid to one of the most important dimensions of parenthood for both mothers and fathers: the need to maintain the family's respectability, in large part achieved through the appropriate behaviour of the children and their parents. This core motivation might be harnessed in the design of interventions to reduce spousal violence, modify negative parenting and encourage sensitive parenting, in order to reduce children's future risk of sexual, physical and/or emotional violence. In Uganda, the investigators are not aware of any parenting programs that deliberately recruit parental couples to complete both single and mixed sex sessions. The Investigators therefore designed a community-based parenting program, - Parenting for Respectability (PfR), - to address this gap in Uganda, and contribute evidence on how a parenting program can address both IPV and VAC. Following careful formative evaluation, the investigators conducted a pre-post study to establish whether there was sufficient evidence of effectiveness to warrant progression to a randomized controlled trial.

The programme has undergone formative evaluation (2014-16), 'Proof of Concept' pre-post outcome evaluation (2016-2019), and with support from Evaluation Fund, is currently being evaluated to assess implementation and scale-up modalities (April 2020-October 2021) in central Uganda. The investment in developing PfR so far has provided important lessons about the acceptability of PfR and how to refine it. Preliminary outcome evidence suggests that a rigorous evaluation of PfR is warranted. The pre-post study has found significant change across primary outcomes for both parent- and child-reports, including large effects for reduced harsh parenting (Cohen's f2 = 0.42, p \< .001) and dysfunctional spousal relationships (Cohen's f2 = 0.28, p \< .001), as well as increased positive parenting (Cohen's f2 = 0.48, p \< .001). The programme has been disseminated widely in Uganda (www.parenting.ug.org), and both government and NGOs have expressed interest to scale it. However, two key uncertainties remain: (i) the optimal way to scale up the intervention in a 'real-world setting', and (ii) whether the evidence of effectiveness would be confirmed through a more rigorous, experimental, evaluation. As a result, this study will combine a rigorous cluster randomised control trial (cRCT) evaluation of PfR with an implementation study using a hybrid type 2 design to examine its effectiveness and cost-effectiveness as well as answer critical contextually relevant implementation science questions. This is essential to ensure that precious resources are not wasted and that there are no harmful unintended consequences from the programme.

Conditions

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Parenting Gender-based Violence Child Maltreatment IPV

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Cluster Randomized Controlled Trial Hybrid Type 2 Evaluation
Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Participants Outcome Assessors
The allocation status of other participating families will be concealed from participants, thus reducing the potential for contamination. Research assistants conducting data assessments and statisticians conducting analysis will be blind to allocation in order to minimise assessment bias. Different groups of research assistants will be employed for outcome assessments and monitoring of implementation fidelity and adherence. Any instances of compromised blinding will be immediately reported. In the case of instances of harm or severe abuse being reported by a participant at any stage of the study, the allocation status of the participant will be un-blinded. All cases of un-blinding will be reported. Because of facilitators' involvement in the programme implementation, blinding will not be possible for service providers. Similarly, of course, participants cannot be blind to their own treatment condition.

Study Groups

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Intervention-Parenting for Respectability

Randomisation in the cRCT will be conducted at the cluster level. PfR is a 16-session manualised programme starting with nine single sex sessions followed by seven mixed sex sessions, delivered once a week by two local facilitators who receive one week's training. Activities were developed specifically for PfR or adapted from other parenting programs, including Project H, Stepping Stones, Mema kwa Jamii, The International Child Development Programme and Parenting for Lifelong Health. The programme addresses four familial processes associated with GBV and VAC: poor parental bonding and child attachment; harsh parenting; inequitable socialisation by gender and parental conflict. A particular goal is to involve fathers, whom most parenting programmes find hard to recruit, and the first nine sessions are delivered in single-sex groups.

Group Type EXPERIMENTAL

Parenting for Respectability

Intervention Type BEHAVIORAL

The programme addresses main challenges of Parenting and builds skills in 4 main areas

1. Poor parental bonding and child attachment;
2. Harsh parenting
3. Inequitable socialisation by gender
4. Parental conflict.

Control-Parenting for Respectability in a nutshell

Randomisation in the cRCT will be conducted at the cluster level immediately after baseline data collection. Parents allocated to the control arm will receive a two-hour structured lecture called Parenting in a Nutshell on parenting and partner relationships. Three topics will be covered: 1) child development; 2) positive parenting; and 3) resolving partner conflicts. Facilitators delivering this lecture will have same/similar expertise with the facilitators engaged in PfR. .

Group Type ACTIVE_COMPARATOR

Parenting for Respectability

Intervention Type BEHAVIORAL

The programme addresses main challenges of Parenting and builds skills in 4 main areas

1. Poor parental bonding and child attachment;
2. Harsh parenting
3. Inequitable socialisation by gender
4. Parental conflict.

Interventions

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Parenting for Respectability

The programme addresses main challenges of Parenting and builds skills in 4 main areas

1. Poor parental bonding and child attachment;
2. Harsh parenting
3. Inequitable socialisation by gender
4. Parental conflict.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

1. Age 18 or older;
2. Primary caregiver responsible for the care of a child between the ages of 10 and 14;
3. Agreement to participate in the PfR programme if allocated to the treatment condition;
4. Provision of consent to participate in the full study.


1. Age 10 to 14 years;
2. Live in the same household as primary caregiver who is part of PfR study;
3. Parent/caregiver gives consent to participate in the study;
4. Provision of consent to participate in the full study.


1. Age 18 or older;
2. Facilitator who is involved in the delivery of the Parenting for Respectability programme;
3. Provision of consent to participate in the full study.


1. Age 18 or older;
2. Involvement in delivery of PfR, or existing leadership role in communities where PfR is delivered;
3. Provision of consent to participate in the full study.

Exclusion Criteria

1. Below Age 18;
2. Not a Primary caregiver responsible for the care of a child between the ages of 10 and 14;
3. Does not Provide consent to participate in the full study.


1. Below Age 10 and above age 14
2. Does not Live in the same household as primary caregiver who is part of PfR study;
3. Parent/caregiver does not gives consent to participate in the study;


1. Below age 18;
2. Facilitator who is Not involved in the delivery of the Parenting for Respectability programme;
3. Does not Provide consent to participate in the full study.


1. Below age 18;
2. Is not Involved in the delivery of PfR, or has no existing leadership role in communities where PfR is delivered;
3. Does not provide consent to participate in the full study
Minimum Eligible Age

1 Year

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Glasgow

OTHER

Sponsor Role collaborator

Oak Foundation

OTHER

Sponsor Role collaborator

Network of European Foundations

UNKNOWN

Sponsor Role collaborator

University of Oxford

OTHER

Sponsor Role collaborator

Makerere University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Dr. Godfrey Siu, PHD

Role: PRINCIPAL_INVESTIGATOR

Child Health and Development Centre, Makerere University

Dr. Jamie M. Lachman, D.PHIL

Role: PRINCIPAL_INVESTIGATOR

University of Glasgow: MRC/CSO Social and Public Health Sciences Unit

Locations

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Wakiso Busukuma and Amuru Lamogi subcounties

Kampala, , Uganda

Site Status

Countries

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Uganda

Provided Documents

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Document Type: Study Protocol

View Document

Other Identifiers

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Uprise2021

Identifier Type: -

Identifier Source: org_study_id