ClinicalTrials.gg
CompletedNCT07771738MLI-SargodhaUpdated Aug 18, 2026

Microbe-Literacy Germ-Watching Workshops for Hygiene and Vaccine Acceptance in Sargodha, Pakistan

An interventional study of Microbe-literacy germ-watching workshop in Vaccination, Hygiene and Vaccine Hesitancy, sponsored by Development Synergies International (Private) Limited. Completed at 1 site in Pakistan. Open to female participants aged 14 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-18.

Sponsored by Development Synergies International (Private) Limited · Not applicable, Interventional, and Health services research

From the registry’s dates

  • Registered 2 years 3 months after the study started (first participant enrolled May 2024, registered Aug 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
1,200
Allocation
Randomized
Ages
14 Years and older
Sex
Female
01

Study summary

This cluster randomized controlled trial evaluated whether a single microscope-based "germ-watching" workshop, delivered by Lady Health Workers (LHWs) to mothers and female caregivers of children under three years, improves hygiene practices, vaccination attitudes and intentions, routine immunization, and trust in LHWs. Twelve Union Councils in Sargodha District, Pakistan, were allocated 1:1 to the intervention or routine services, with outcomes measured by structured baseline and endline surveys and facility immunization records.

Read the detailed description

In intervention clusters, LHWs used portable microscopes (>=400x) to show caregivers the microorganisms present in their own household water and food samples during a single 120-minute workshop for 25-30 participants, linking observed microbes to hygiene and vaccine-preventable disease. Control clusters received routine LHW services and standard national health messaging. Allocation used restricted, covariate-constrained randomization at the Union Council level; outcome data entry and analysis were blinded to allocation. Analyses accounted for clustering.

02

Conditions studied

  • Vaccination
  • Hygiene
  • Vaccine Hesitancy
  • Health Knowledge Attitudes and Practice

Keywords

  • Microbe literacy
  • Germ watching
  • Lady health workers
  • Immunization
  • Handwashing
  • Health education
  • Cluster randomized trial
03

In context

Vaccination Hesitancy

121 studies on the registry are indexed under Vaccination Hesitancy; 14 are open to participants now.

This study's enrollment of 1,200 is above the median of 516 across 98 interventional studies indexed under Vaccination Hesitancy.

Browse Vaccination Hesitancy studies →

Lead sponsor

This is the only study on the registry with Development Synergies International (Private) Limited as lead sponsor.

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

04

Who can participate

Ages eligible
14 Years and older
Sexes eligible
Female
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

  • Mother or female caregiver, permanent resident of the study area
  • At least one child aged under 3 years
  • Written

Exclusion criteria

Exclusion Criteria:

  • Already enrolled in a similar intervention
  • Unable to participate due to physical/psychological constraints
  • Intending to relocate during the study period
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
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
1,200 participants (actual)

Study arms

  • Experimental
    Microbe-literacy workshop (Intervention)

    Routine LHW services PLUS a single 120-minute microscope-based germ-watching workshop.

    Behavioral: Microbe-literacy germ-watching workshop

  • No intervention
    Routine services (Control)

    Routine LHW services and standard national health messaging; no workshop

Interventions

  • BehavioralMicrobe-literacy germ-watching workshop

    Group demonstration (25-30 participants) using portable microscopes to visualize microorganisms in participants' own environmental samples, linked to hygiene and immunization messages

06

What researchers measure

Primary outcomes

  1. Proportion of caregivers/children reporting always washing hands (self-reported)

    Percentage of caregivers (and their children) reporting they "always" wash hands with soap / before eating, from a structured interviewer-administered survey item, compared between arms.

    Time frame: Baseline and 4 months (endline, immediately after the intervention period)

  2. Third-dose oral polio vaccine (OPV3) coverage (facility records)

    Percentage of index children with a documented third dose of oral polio vaccine, ascertained from facility immunization records, compared between arms.

    Time frame: 4 months (endline)

  3. Proportion with self-reported completion of the age-appropriate immunization schedule

    Percentage of caregivers reporting the index child had received all age-appropriate vaccinations (structured survey item), compared between arms.

    Time frame: Baseline and 4 months (endline)

Secondary outcomes

  1. Proportion reporting high trust in Lady Health Workers

    Percentage of caregivers responding "yes, a lot" to a single-item survey question on trust in Lady Health Workers for vaccine information, compared between arms.

    Time frame: Baseline and 4 months (endline)

  2. Proportion aware that germs cause infectious disease

    Percentage of caregivers identifying germs (rather than, e.g., "bad weather") as the cause of infectious disease on a survey item, compared between arms.

    Time frame: Baseline and 4 months (endline)

  3. Proportion perceiving vaccines as safe

    Percentage of caregivers responding "yes, safe" to a survey item on perceived vaccine safety, compared between arms.

    Time frame: Baseline and 4 months (endline)

  4. Proportion intending to vaccinate ("very likely")

    Percentage of caregivers responding "very likely" to a survey item on intention to vaccinate the child in future, compared between arms.

    Time frame: Baseline and 4 months (endline)

  5. Proportion willing to recommend vaccination to others

    Percentage of caregivers responding "yes" to a survey item on willingness to recommend vaccination to other mothers, compared between arms.

    Time frame: Baseline and 4 months (endline)

07

Study locations

1 site
  • Community Study
    Sargodha, Punjab Province 40100, Pakistan
08

References and documents

Individual participant data

Plan to share: Undecided — De-identified participant data available from the corresponding author on reasonable request.

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from May 2024 to primary completion in Aug 2024, 3 months.

Of 82 non-industry interventional studies with no phase under Vaccination Hesitancy, half reached primary completion within 6 months of starting (the median), counting those still running; a quarter within 3 and three quarters within 14. This study's 3 months is below that.

Counting every sponsor, half of 83 studies reached it within 5 months; a quarter within 2 and three quarters within 14.

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

Registered
Aug 11, 2026
First posted
Aug 18, 2026
StartActual
May 1, 2024
Primary completionActual
Aug 31, 2024
CompletionActual
Aug 31, 2024
Last update
Aug 18, 2026
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 Aug 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07771738
Lead sponsor
Development Synergies International (Private) Limited
Collaborators
Microbe Literacy Initiative, National University of Science and Technology, Pakistan
Responsible party
Sponsor
First posted
Aug 18, 2026
Start date
May 1, 2024
Primary completion
Aug 31, 2024
Completion
Aug 31, 2024
Last update
Aug 18, 2026

Oversight

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

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This study is completed, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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