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Child AbuseNCT03374761

Families First Program Evaluation in Indonesia

A study testing Families First Home Visiting Program in people with Child Abuse and Parent-Child Relations, run by McGill University at 1 site in Canada.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Families First Home Visiting Program (Families First) is a parenting support program anchored on children's rights that gives parents clear guidance on child development, parenting, and positive discipline practices. Read more about this study

Who is it for?
Ages 14 years and older, women only
Conditions the study is for
Child Abuse, Parent-Child Relations
What is being tested?
Families First Home Visiting Program
Could I receive a placebo?
No, everyone receives an active treatment
How many people
720 participants
Where
1 siteCanada
Study dates
22 Mar 2017to 31 Aug 2019
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 14 years and older
  • Women only
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • Have at least one child aged up to 7 years, regardless of whether the child is their biological child or not;
  • Have at least one of the risk factors associated with the placement of children into residential care: live below the government poverty line; be a single and teenage mother; father or mother has migrated/or mother is considering migration;
  • Have basic needs met or be referred to social protection program before start of program;
  • Reside in the village;
  • Not been previously identified as having cognitive impairment
  • Able to speak and read in Bahasa;
  • Have never engaged in another parenting program;
  • Does not plan to move from this village for a year ahead

Who cannot join

None listed.

Trial locations and contacts

1 site in 1 country.

Canada1 site
  • Division fo Clinical epidemiology

    Montreal, Quebec, H3A 1A1

Other trials in Canada

About this study

Official title: Families First Positive Discipline for Everyday Parenting With Home Visiting Program in Indonesia

Families First Home Visiting Program (Families First) is a parenting support program anchored on children's rights that gives parents clear guidance on child development, parenting, and positive discipline practices. Families First is an adaptation of the Positive Discipline in Everyday Parenting (PDEP) Program for the West Java context. This trial aims to evaluate the effectiveness of Families First. This is a pragmatic, delayed-entry, parallel-group, stratified, cluster-randomized controlled trial in a real-world setting. Twenty rural and urban villages in the Cianjur district of Indonesia, involving 720 caregivers of children up to 7 years of age, are randomized to two parallel arms. Villages receive either a parenting program consisting of 10 group sessions and 4 home visits or the standard community health and social services. After completion of the trial period, the delayed group is offered the program. The primary outcome is self-reported frequency of corporal/physical and emotional punishment. The secondary outcomes are indicators of involved and positive parenting. Concurrent process evaluation and qualitative research are conducted to identify program satisfaction and facilitators and barriers to the implementation. Outcome data are collected immediately after the intervention and six months later. The results will be used to inform a violence prevention strategy in West Java and possible scale up in of the intervention in Indonesia.

Read the detailed description

Aims and objectives The primary objective of this study is to compare, among caregivers of children aged 0-7 years in Cianjur district, Indonesia, the effectiveness of the Families First Program in reducing rates of violent discipline episodes in the home in comparison to rates observed under the standard community health and social service provision. The study will also identify unintended positive and negative effects of this program; determine facilitators and barriers to its implementation in this context; and assess facilitators, mentors, and families' satisfaction with the program.

Site eligibility Data will be collected across 20 villages or clusters that represent the general population in four sub-districts (Campaka, Ciranjang, Karang tengah, and Naringgul) in Cianjur district, West Java Province, Indonesia. Selected villages will consist of (a) rural and urban/peri-urban communities; (b) not been exposed to the Families First Program; (c) reachable within a 1-hour driving distance of the sub-district office and 1-8 hours driving distance of the district capital; (d) located at ample distance from other clusters; and (e) local political leaders provide approval for the intervention and the evaluation.

Randomization Stratified randomization will be used to select 20 clusters among the eligible 38 study clusters in rural and urban settings in the four sub-districts in a 1:1 ratio for the intervention and the control arms. Clusters will be randomized to avoid the resentment or contamination that might occur as a result of delivering the intervention to some families but not others in the community. Randomization will be done in a Random Allocation Ceremony led by the research team and attended by the chiefs from all participating villages as well as staff from the implementing agency. The ceremony will follow a step-by-step lottery and documentation procedure that includes the use of 20 sequentially numbered, opaque, sealed and stapled envelopes independently prepared by the lead investigator. Aluminium foil inside the envelope will render the envelope impermeable to intense light. The ceremony will be video-recorded. Eligible families will be identified before randomly assigning villages.

Measurement strategy The outcome measures for this study are given in the measurement section of the registration document. The original measurement strategy was to use full measures that have already been applied in this field. Piloting of the original plan indicated that this would not be feasible as there were too many items, many of which would not be appropriate or relevant to the context. Instead, the measurement strategy was to use outcome indicators: single items; indices by cumulating responses over several related items; or full measures/subscales with total scores validated using Rasch analysis.

Socio-demographic covariates Socio-demographic characteristics that will be documented include: a) Child: age, gender, orphanhood status, siblings, physical health, and school status; (b) Mother/caretaker: age, gender, marital status, education level, physical and mental health, ethnicity and cultural background, school/employment status; (c) Family: urban/rural location \& type of residence, household structure, family structure, economy, and functioning.

Qualitative and process evaluation assessments Linked qualitative methods will be used to develop and validate data collection measures (pilot) and to add depth and understanding of process and outcomes. During the randomized trial stages, they will explore caregivers' and implementers' experiences in the program and how service delivery, socio-economic, cultural, and other factors may impact the effectiveness and scalability of the intervention. Qualitative methods (in Bahasa and Sundanese) include semi-structured interviews with caregivers, implementers (Save the Children/non-governmental organization staff, mentors, and facilitators) and community leaders; focus group interviews with participating caregivers and implementers; observation of group sessions; record analysis; and visual methods.

Facilitator's tracking forms will be used to record attendance and level of engagement by caregivers, as well as the extent to which facilitators followed the program manual. Process evaluation outcomes will be assessed through checklists to track implementation fidelity, program exposure/attendance, and a brief program satisfaction questionnaire for caregivers in intervention sites, facilitators, and mentors post-intervention. Implementer records of program attendance and fidelity in the delivery of the intervention (as assessed by observation of sessions by mentors) will also be reviewed.

Statistical analysis and sample size calculation The study is powered to detect a change considered to be both significant clinically and plausible on the primary outcome. A sample size of N = 720 families will allow measuring a reduction of 15.2% in parent-reported use of violent discipline at home from the initial estimated prevalence of 30% (SKTA 2013) with an α level of 0.05 and 90% power, assuming 0.02 intra-class correlation and 80% participation rate. While each family will likely have more than one child, the outcome concordance across children is likely to be very high (>0.8) and so the sample size calculation considers the number of families, recognizing that the unit of analysis will be the child.

Types of analysis There will be only one analysis when all participants have been randomized. There will be administrative analyses done to ensure data accuracy on a continual basis. A baseline table reflecting the demographic profile of the households and caregivers by arm will be compiled.

The primary outcome is frequency of three types of punishment practices in the past month which will be aggregated into a cumulative rate of number of punishments over days. For comparative purposes, the primary outcome will be evaluated as any- vs. non-punishment. This rate will be ascertained for all participants in both trial arms three times. The main analysis will be logistic regression using generalized estimating equations (GEE) to nest families within villages to test the main hypothesis related to the superiority of the program in reducing the rate of physical and emotional punishment over the period of the study. Outcomes will be measured at baseline, end of intervention, and follow-up (i.e., 6 months after end of intervention). The primary comparison is at the end of the intervention; comparisons at follow-up are considered exploratory. The superiority of the program will be tested by including main effects for program and for time along with a program by time interaction. The linearity of the association with time will be considered to allow for the possibility of non-linear associations. Variables which reduce variance in the outcome will be considered for inclusion (sex and position (parent or child) of the reporting family member, number of children in the family, etc.). Although confounding is not expected to be an issue due to the randomization, villages will be compared on key factors and any variables showing large imbalances by randomization group will be added to the model. The investigators will adopt an intention-to-treat principle to analyze all outcomes and all persons will be analyzed in the groups to which they were randomized. A secondary analysis will estimate the impact of the program the other relevant outcomes. Program effects will also be examined using GEE to adjust for clustering of members within families and families within villages. Counts will be analyzed with poisson regression, binary outcomes with logistic regression and continuous scales with linear regression. The investigators will conduct a gender-based analysis (sex of the child) for exploratory purposes. The investigators will also explore whether families with more children or children of different age groups, or families with differently-abled children respond differently to the program. Another sub-group analyses will explore the impact of the intervention among people in single-headed households, first-time parents, and teenage parents. Analysis and reporting of the results will follow the CONSORT guidelines for reporting randomized controlled trials. Preliminary findings will be shared with the Advisory Committee and interpreted in the context of relevant policies.

Data management and monitoring Tablet-based questionnaires will be administered orally to caregivers in their homes. The Census and Survey Processing System (CSPro), a widely-used public domain software package that allows for collection of data and later uploading to the secure server, will be used for entering, editing, and tabulating data. An index child will be randomly selected at the beginning of the baseline interview.

The study will be monitored for quality, contextual appropriateness, and regulatory compliance. An independent advisory committee composed of academics and specialists with an expertise in child protection in Indonesia from government, non-governmental, and donor agencies will participate in the continuous monitoring of the study. Program implementers will monitor the intervention through facilitators and mentors' weekly meetings, and local visits by other program staff. Any adverse events observed by researchers or implementers will be assessed to decide whether additional investigation or a modification of the intervention may be indicated.

Being tested
Families First Home Visiting Program
Keywords
child abuse, parenting, low and middle income countries, child discipline, Indonesia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Families First Home Visiting ProgramOther

    10 group sessions and 4 home visits with community facilitators emphasizing positive parenting

Study groups in NCT03374761
Study groupRoleWhat they receive
Families First Home Visiting ProgramExperimental10 group sessions conducted weekly and 4 home visits for the duration of the program. Sessions and visits of the Families First Home Visiting Program cover child development, parenting skills, parent-child communications, and positive discipline practices. The intervention is delivered by para-professional community facilitators, trained in the program.
Receives: Other: Families First Home Visiting Program
Control GroupNo interventionThe control group receives the standard, government run, services provided by community health workers in West Java. Once the evaluation of the intervention arm is completed, participants in the control arm will be offered the intervention.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in frequency of physical and emotional punishment at 3 and 6 months

    Self-report frequency in the past month of use of physical discipline including harsh physical discipline, and verbal/emotional discipline.

    Measured: Baseline, post-intervention (3 months), and 6 months follow-up

Secondary outcomes (4)
  1. Positive and involved parenting

    Positive Parenting Subscale (6 self-report items) and 1 single self-report item from Involvement Subscale of the Alabama Parenting Questionnaire (APQ).

    Measured: Baseline, post-intervention (3 months), and 6 months follow-up

  2. Positive discipline

    Four self-report items adapted from the International Society for Prevention of Child Abuse and Neglect Child Abuse Screening Tool (ICAST) Nonviolent Subscale.

    Measured: Baseline, post-intervention (3 months), and 6 months follow-up

  3. Opinion on discipline

    Two items from the International Society for Prevention of Child Abuse and Neglect Child Abuse Screening Tool (ICAST)-Parent.

    Measured: Baseline, post-intervention (3 months), and 6 months follow-up

  4. Setting limits

    2 items from the Setting Limits Subscale of the Parenting Young Children (PARYC)

    Measured: Baseline, post-intervention (3 months), and 6 months follow-up

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Dec 2017
  2. Study start22 Mar 2017
  3. Primary completion24 Mar 2018
  4. Study completion31 Aug 2019 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Model description
Stratified, clustered randomized pragmatic trial
Masking
None (open label)
Enrolment
720 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03374761
Sponsor's protocol ID
A10-B53-16B
Status last verified
Aug 2019
First submitted
30 Nov 2017
Last updated
7 Aug 2019
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Ruiz-Casares M, Lilley S, Thombs BD, Platt RW, Scott S, Isdijoso W, Hermanus E, Andrina M, Mayo N. Protocol for a cluster randomised controlled trial evaluating a parenting with home visitation programme to prevent physical and emotional abuse of children in Indonesia: the Families First Programme. BMJ Open. 2019 Jan 15;9(1):e021751. doi: 10.1136/bmjopen-2018-021751.

    PubMed 30782674

Questions about this trial

What is this clinical trial studying?

A study testing Families First Home Visiting Program in people with Child Abuse and Parent-Child Relations, run by McGill University at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 7 Aug 2019. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in frequency of physical and emotional punishment at 3 and 6 months (time frame: Baseline, post-intervention (3 months), and 6 months follow-up). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03374761, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Aug 2019.

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