Medical Coordination
Tracking appointments, meds, and follow-ups.
Making caregiving visible, shared & sustainable.

This was an academic exploration focused on understanding caregiver burden and designing responsibly within complex social systems.
As a student design team, we examined the gap between “shared” care and lived responsibility to understand how care actually functions inside Indian families, and where existing support systems are failing caregivers.

A healed bone in early human remains signified something radical: someone chose to care.
Civilisation did not begin with tools or weapons, it began with support. Caregivers embody that same social infrastructure today. Designing for them strengthens the system that holds families together.
Caring for an elderly family member involves more than physical help. It often includes:
Tracking appointments, meds, and follow-ups.
Managing reports, prescriptions, insurance, and consent.
Balancing work, family, and personal health.
Finding, hiring, and coordinating trained caregivers.
While providing care is culturally expected to be shared, it often drifts to one person, without explicit discussion or support.
Rather than treating caregiving as a set of isolated tasks, we explored Khayal as an ecosystem that supports both:
“Somebody who could understand me and just hear me out.”
Access curated content & create/join communities to organise events, share resources and talk to people with similar experiences.
“Everything is in my head”
Store & organise documents by dependent and make sharing tasks with family easier.
“I’ll have to quit my work or if we don’t have a way to manage without me working, then I have to hire someone.”
Browse Certified Caregiver Matches for focused attention at home, or discover local care centres close to you.
“Everyone is well-meaning, but when you’re the one nearby, all the responsibility falls on you.”
Make daily tasks visible and share with an extended care network to build healthy boundaries around care.




Recognising that caregiving affects emotional wellbeing, routines, social life, and finances beyond physical assistance, we combined caregiver conversations, surveys, and secondary research to validate patterns across sources.

These findings were consolidated into a structured research report documenting our methodology, analysis, and key insights, which informed the direction of our design exploration.
Read the full reportResearch reportOpen
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03These insights helped us identify opportunity areas where design could meaningfully support caregivers.
We explored multiple ways a digital product could support caregivers in managing responsibilities and coordinating care.
Five early concepts were developed and shared with caregivers to understand what felt useful, realistic, and relevant to their daily lives.

Their feedback helped us identify which ideas resonated most and which ones needed refinement or deprioritisation.
Caregivers liked being able to see care details, documents, and responsibilities in one place, especially when multiple people were involved.
Caregivers responded positively to professional help options that could adapt to changing schedules. On-demand support was seen as a way to regain personal time and flexibility.
Caregivers appreciated solutions that acknowledged stress and provided a community for them to share and bond through similar experiences.
Concepts that addressed only the logistics without acknowledging emotional load felt incomplete.
Caregivers found rigid, long-term care plans unrealistic; they liked concepts that adapt to changing health, work, and family needs.
Using our research insights and testing feedback, we established a structured information architecture and user flows to give shape to Khayal’s caregiver support vision.


Caregivers want one place to access and manage care information, rather than relying on scattered messages or memory.

Caregivers want an easy way for family members to see ongoing responsibilities and step in when needed.

Caregivers want to find trustworthy in-home help when required, without long-term commitment or loss of control.

Caregivers want accessible respite options close to home.

Caregivers want guidance that feels timely and personal, that responds to both the patient’s needs and their own.

Caregivers want to feel heard and understood. They need a space to share experiences, ask questions, and express stress without judgment.
The research pointed towards a potential direction for caregiving: making care more visible, easier to share, and more supportive for the person carrying the coordination.
A care coordination system that brings shared responsibilities, flexible support, and emotional care into the same experience.

Future exploration would need to build trust around privacy, reliable care services, and the different roles families play in caregiving.
I began by designing with empathy, but along the way I understood the difference between feeling for someone and designing to actively support them.
Initially, we framed the solution as an app. Over time, I realised the interface was only a vehicle. If I approached this again, I would define the system first with roles, behaviors, incentives and let the product emerge from that foundation.
While testing concepts, I would go beyond usability and treat emotional safety as a primary constraint, asking consistently if a feature would reduce stress or amplify it.