Who we partner with

  • Universities & research labs: co-design protocols, co-author papers, train students.
  • Government & public health agencies: plan screenings, target interventions, evaluate programs.
  • Hospitals & clinics: embed context in follow-ups, adherence, and care pathways.
  • NGOs & community orgs: run field pilots with safe, language-inclusive intake.
  • Businesses & employers: workplace health studies and context-aware wellness pilots.

What you get

  • Co-designed studies using our living dataset (Bantu Atlas) and tools.
  • Authorship & credit on briefs, dashboards, and publications.
  • Anonymised data access under strict governance.
  • Field toolkits (intake forms, voice prompts, translations).
  • Capacity building for staff and students.
  • Impact tracking that respects culture and constraints.

How we work with partners

A steady, ethical path from first call to impact. We keep collaboration simple, rigorous, and human, so your team can move from question to action without noise

  • Introduction & fit

    We start with a 30-45 minute call to understand your question, population, timelines, and ethics requirements, and to confirm mutual fit. You’ll meet a single point of contact who stays with you end-to-end.

  • Scope, protocol & ethics

    Together we shape the research protocol using our approved intake and consent flows, align on data protections, and confirm IRB/ethics pathways (yours or ours). We finalise roles, sampling, tools, and success measures.

  • Pilot & field support

    We run a 6–12 week pilot with your team: onboarding, field training, QA, and weekly check-ins. Bantu Atlas captures context; Pattern Ops surfaces meaningful shifts; Asabe tone guidelines are set where relevant.

  • Insight, publication & continuity

    We co-review findings, produce briefs or papers (authorship credited), and map next steps, scale, follow-up cohorts, or program integration. We schedule quarterly reviews to maintain momentum and quality.

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Methods and governance

We design for dignity and usefulness. Participation is consent-based; data is anonymised, access-controlled, and never sold. We collect only what’s needed for care and research and delete what we don’t need. Partners work under shared protocols and ethics review.

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Current priority themes

We co-design studies around lived context and measurable change. Below are the themes we’re actively prioritising with partners across regions, spanning daily routine, environment, and clinical realities.

  • Nutrition and daily food patterns
  • Sleep and recovery
  • Movement by routine and gym contexts
  • Stress, coping rituals, and energy load
  • Maternal, perinatal, and caregiver burden
  • Chronic-care adherence (e.g., hypertension, diabetes)
  • Faith and seasonal rhythms (including fasting)
  • Urban time-poverty, commute, and service access
  • Environmental conditions (heat, air quality, noise)
  • Emotional and mental health signals (mood, isolation)
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Let’s run a study together

Bring your question. We’ll co-design protocols, handle ethics and field tools, analyse with Bantu Atlas and Pattern Ops, and publish together.

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