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Advance Health Related Quality of Life Clinical Research and Care

Assess and improve health related quality of life (HRQL) by gathering patient reported outcomes (PROs) and supplementary health data, while engaging patients in their care.
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Zamplo Research In Action

1-Sep-15-2023-05-57-49-1644-PM
Remote Clinical Care

The PATH Project

  • Determining if systemic symptom monitoring via PROMs during radiation delivery improves clinical outcomes and reallocates resources meaningfully.
  • Collecting PROs and facilitating proactive symptom management through Zamplo Research.
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Data Driven Measurement Based Care

The iPathPort Project

  • Deploying a patient-centered platform.
  • Aims to better understand individual treatment trajectories and barriers to accessing services within the addiction system of care.
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Validating Care Pathway

Radical Mental Health Doula Project

  • Aims to apply the expanded radical doula model as an innovative framework of support in mental health.
  • Uses PROMs, collected through Zamplo Research to validate a new care pathway.
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Collect PROs

Create and send standardized questionnaires to patients and study participants to collect PROs. 

Ask participants a standardized set of questions, like symptoms of depression or pain and choose from multiple question types including single and multi-item scales.

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Choose from Multiple Question Types
Choose from various question types including "single and multiple selection, symptom slider, and survey table.
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Create Branching Paths
Select branching options: next question, skip to question, and skip to question based on selected option.
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Set Survey Schedules
Send out a survey once or for frequent completion at a certain point throughout the study, after a specific event occurs, or to a certain group.
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Collect Participant Consent
Attach consent forms to collect consent once per survey, once per survey instance, or once per participant.

Collect Supplementary Health Data

As PROs are just one piece of information to help you enhance patient care, Routines are beneficial if you want to collect supplementary data to further inform clinical care and research.

Routines, captured as participant Entries, allow you to gather different points of health information, tracked over time.

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HRQL Data That Can Be Tracked

Symptoms

e.g., fatigue, nausea, anxiety

Symptoms

Medications & Supplements

e.g., codeine, fluoxetine, vitamin D
Medications & Supplements

Functioning

e.g., activities like yoga and painting
Functioning

Health Data

e.g., body temperature, weight, hours of sleep
Health Data
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Engage Patients

Engage patients in their care as they document their health journey using the Zamplo App. Patients can keep track of symptoms, activities, health data, and medications, using a desktop or mobile device.

Patients retain control of their data and can access their personal health information to make more informed decisions.

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Share Health Resources
Upload and share health resources (including websites, documents, and videos) to all participants or select individuals.
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Community of Peers
Individuals can connect one-to-one with others with the same diagnosis to share experiences, wellness and advocacy tips, and more.
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Caregiver Access
Participants can invite a caregiver or care team member to help contribute, manage, and view health information.
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Participant Data Ownership
Data inputted into the Zamplo App is owned by the participant, allowing them to contribute data to future studies.

Data Security and Ethics

Commitment to privacy and security is at the core of Zamplo Research.

All infrastructure is managed by Zamplo Software service. All data is encrypted and resides in Canada. Data export can be performed only by authorized users of your study team.

Unique to Zamplo Research, participants own their data, allowing them to contribute to studies in the future and keep their data for life.

Advance HRQL Research

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