ClinicalTrials.gg
Not yet recruitingNCT06431321Updated May 29, 2024

Evaluation of a 2-session Parent Training Programme for Caregivers of Younger Children in Zimbabwe

An interventional study of Tabudira Parenting Intervention for Early Childhood Development and Nutritional guide for younger children in Child Maltreatment, sponsored by University of Cape Town. Not yet recruiting at 1 site in Zimbabwe. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-05-29.

Sponsored by University of Cape Town · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Primary completion was expected by Aug 2024, 2 years 2 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
240
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

A pilot, exploratory cluster Randomised Controlled Trial (RCT) with two arms will be conducted to test a two-session parent training programme for caregivers of children enrolled in early childhood development classes in Harare Zimbabwe. The Parenting for Lifelong Health programme for Young Children together with the Mikhulu Trust Book Sharing Programme for Young Children will be adapted into a two-session version programme named Tabudirira Parent Training Intervention for Early Childhood Development.

The RCT aims to assess the following objectives:

Can the programme reduce child maltreatment? Does the intervention improve parent-child engagement with reading material? How best can the 2-session programme delivery be optimised?

Read the detailed description

A pilot, exploratory cluster Randomised Controlled Trial (RCT) with two arms will be conducted to test a two-session parent training programme for caregivers of children enrolled in early childhood development classes in Harare, Zimbabwe. The Parenting for Lifelong Health programme for Young Children together with the Mikhulu Trust Book Sharing Programme for Young Children will be adapted into a two-session version programme named Tabudirira Parent Training Intervention for Early Childhood Development.

The RCT aims to assess the following objectives:

Can the programme reduce child maltreatment? Does the intervention improve parent-child engagement with reading material? How best can the 2-session programme delivery be optimised?

The RCt will have 2 arms with 120 caregivers /arms. The intervention will be a 2-session parent training programme while the control is a 2-session nutrition knowledge dissemination workshop delivered over 2 sessions.

02

Conditions studied

  • Child Maltreatment

Keywords

  • Child Maltreatment
  • Parenting
  • Violence Against Children (VAC)
  • Prevention
  • Parenting Intervention
  • Early Childhood Development (ECD)
03

In context

Lead sponsor

University of Cape Town is the lead sponsor of 116 studies on the registry; 14 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Aged 18 years and above.
  • Be a caregiver to a child enrolled in Early Childhood Development Grade A at a school in Harare Northern Central School district.
  • Live with the child for a minimum of 5 days/ week.
  • Provide before any study proceedings.

Exclusion criteria

Exclusion Criteria

  • Aged below 18
  • A child enrolled in a school outside Harare Northern Central School District
  • Child not enrolled in Early Childhood Development Grade A
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
240 participants (estimated)

Study arms

  • Experimental
    Parent training intervention

    The Tabudirira Parenting Intervention for Early Childhood Development will be delivered to parents of children aged 4-5 years in Harare, Zimbabwe. Trained facilitators will deliver the programme face to face, and a group of 15 parents will have 3 facilitators. The facilitators comprise of teachers working as guidance and counselling coordinators and psychology graduates. The programme consists of 2 sessions that will be delivered once a week over 2 weeks, with each session lasting 2.5 to 3 hours. The session will have various activities which focus on learning from each other and practising positive parenting behaviours. At the end of each session, parents will receive a home activity which allows them to practise the content taught during the session. At the end of session 2 parents will receive a parent handbook with the summary of the 2 sessions. Schools will be used as venues and the facilitators will receive ongoing mentoring and coaching during programme delivery.

    Behavioral: Tabudira Parenting Intervention for Early Childhood Development

  • Active comparator
    Control

    The control group (8 groups with 15 parents each) will receive a one-hour session on nutrition with facilitators trained by a nutritionist focusing on children aged 4-7 years. The parents will also receive a nutrition handbook. Zimbabwe is faced with the triple burden of malnutrition: underweight, micronutrient deficiencies and overweight. There is an ongoing need to protect and promote diets, services and practices through a multi-systems approach that supports optimal nutrition, growth, and development for all children, using a parent support group can help achieve the goal. The nutrition programme has no components of positive parenting or links to the reduction of violence against children but will serve as a placebo control for the attention received by parents.

    Other: Nutritional guide for younger children

Interventions

  • BehavioralTabudira Parenting Intervention for Early Childhood Development

    2 session programme delivered weekly over 2 weeks using group-based delivery aimed at reducing child maltreatment, improving parenting behaviours and parent's mental health.

    Also known as: Parenting for Lifelong Health Young Children combined with Mikhulu Trust Book Sharing Programme - 2-Session Version

  • OtherNutritional guide for younger children

    2 session programme delivered weekly over 2 weeks aimed at providing parents with nutritional education to help provide maximum nutrition to the growing child

06

What researchers measure

Primary outcomes

  1. Changes in frequency of child maltreatment:

    The International Child Abuse Screening Tool-Trial version (ICAST-T) measures the occurrence of respondents' discipline behaviour towards the child

    Time frame: 6 weeks

Secondary outcomes

  1. Changes in attitudes towards harsh parenting

    Changes in attitudes towards harsh parenting will be measured using two items from the ICAST-T measure used in measuring the primary outcome. The questions will seek to understand parental attitudes towards harsh discipline for example: In the past 6 weeks, how often did physical discipline seem like the only option for stopping bad behaviour?

    Time frame: 6 weeks

  2. Changes in not knowing what to do when a child misbehaves

    will be measured using 1 item from the ICAST-T the question: In the past 6 weeks, how often did you not know what to do when your child misbehaved

    Time frame: 6 weeks

  3. Spending time with child, praising, naming emotions

    The Parenting Young Children Questionnaire (PARYC) has 9 items that contain statements of parenting behaviours that caregivers rate on a Likert scale from 1 (not at all) to 7 (most of the time). Two dimensions of the PARYC will be measured: Supporting Good Behaviour (e.g., "Notice/Praise good behaviour") and Setting Limits (e.g., "Stick to your rules"). The items included in the current questionnaire (Cronbach alpha 0.86). are informed by the metric invariance analysis of the measure done in a preceding study, pending publication. The preceding study measured the prevalence of violence against children and its correlates. The highest possible score is 63 indicating more parent-child engagement compared to the lowest possible score of 9 indicating fewer parent-child engagements.

    Time frame: 6 weeks

  4. Changes in time spent engaging the child in book sharing

    Two items, similar in structure to those in the PARYC, will be used to assess this e.g. How often do you spend time book sharing with your child?

    Time frame: 6 weeks

  5. Changes in caregiver mental health

    The Shona Symptoms Questionnaire (SSQ-14) will be used to assess parental mental health before and after the programme. The SSQ is a 14-item screening tool for common mental disorders and has a reliable internal consistency (0.85). It asks about symptoms such as thinking too much, failing to concentrate, work lagging, insomnia, suicidal ideation, unhappiness and so on, over 1 week. Highest total possible score of 14 indicates floundering parental mental health while a score of 0 indicates flourishing parental mental health

    Time frame: 6 weeks

  6. Changes in work-family conflict

    The Multidimensional Measure of Work-Family Conflict (MMWFC) measures work-family conflict on three constructs: time, strain and behaviour. The scale has 12 items, with responses on a 7-point Likert scale ranging from strongly disagree to strongly agree. The following are examples of items in the questionnaire: my work keeps me from my family activities more than I would like, I am often stressed from my family responsibilities, and I have a hard time concentrating on my work. The internal reliability was 0.92 in phase 1. The highest possible score is 84 indicating increased work-family conflict compared to 12 which is the lowest possible score indicating better work-family balance.

    Time frame: 6 weeks

  7. Changes in Knowledge of Child nutrition

    : Four questions will be adapted from the Food and Agriculture Organisation of the United Nations guidelines for assessing nutrition-related knowledge, attitudes, and practices. The questions will assess the practices of the child's intake of healthy (2 items) and unhealthy snacks (2 items): How many times a day does your child eat candy? The items will be measured on a 6-point Likert scale ranging from Never to 6 times a day. The healthy eating scores will be reverse scored. The highest possible total is 24 indicating poor snacking practices compared to the lowest possible score of 4 for healthy snacking practices.

    Time frame: 6 weeks

Other outcomes

  1. Implementation Outcomes

    Barriers and enablers to delivery Barriers and enablers to parent engagement (attendance, homework completion)

    Time frame: 6 weeks

07

Study locations

1 site
  • Harare Northen Central School District
    Harare, Zimbabwe
    • Marian Mazingi District Official: Ministry of Primary and secondary Education · Contactmmazingi@ymail.com · +263 772 864 277
08

References and documents

Individual participant data

Plan to share: Yes — Ziva Hub Anonymised Individual Participant Data

Supporting information: Study protocol, Statistical analysis plan, Informed consent form

Time frame: 2026

Access criteria: Open

Data sharing details ↗ · zivahub.uct.ac.za

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Jun 2024; primary completion for Aug 2024, 2 months later.

How these figures are worked out, and which studies are left out of them.

Registered
May 8, 2024
First posted
May 28, 2024
StartEst.
Jun 7, 2024
Primary completionEst.
Aug 15, 2024
CompletionEst.
Sep 5, 2024
Last update
May 29, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 29, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06431321
Collaborators
Parenting for Lifelong Health, Mikhulu Trust, Clowns Without Borders South Africa, Ministry of Primary and Secondary Education Zimbabwe
Responsible party
Noreen Wini Dari (Principal Investigator, University of Cape Town) — Principal investigator
First posted
May 28, 2024
Start date
Jun 7, 2024 (estimated)
Primary completion
Aug 15, 2024 (estimated)
Completion
Sep 5, 2024 (estimated)
Last update
May 29, 2024

Study contacts

Noreen Wini Dari, MSc
Contact
wndnor001@myuct.ac.za
+263 718 886340
Cathrine Ward, PhD
Contact
Catherine.Ward@uct.ac.za
+27 21 650 3422
Noreen Wini Dari, MSc
principal investigator · University of Capetown

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in May 2024. You cannot join it, but the record below documents what was studied.

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