Future study participants / Programme outline
Participant permissions
Study information, permissions, compensation and withdrawal. No enrolment or consent is collected here.
A separate, informed decision.
A future study must provide its own participant information and permissions before collection. This outline does not recruit participants or obtain consent. Using the consumer app is not consent to research or commercial model training.
Earlier LifeFrom commitments continue to apply to existing app records. A new programme cannot silently change their permitted uses.
Explain the actual study.
- Name the responsible entity, study purpose, eligibility, geography, duration and contacts.
- Describe each source, task, device, visit and follow-up, including expected time and any clinical involvement.
- Explain who receives what, identifiability, intended training or evaluation uses, retention and transfer arrangements.
- Identify the legal basis and any study-specific ethics or regulatory review required before recruitment.
Specify the uses, not just the upload.
Participant-authorized exports are a possible acquisition route. Their source and applicable restrictions still need review. Permission to upload a record does not by itself establish every downstream licensing or training right.
Permission records must identify the version shown, purpose, data categories, recipients or recipient categories and participant decision. Collection, research, commercial licensing and training uses should be described distinctly where applicable.
Make the exchange clear.
The study must disclose compensation, payment timing, eligibility and treatment of partially completed tasks before participation. No payment amounts, free tests or clinical benefits are promised by this page.
A participant should not be penalized for an unfavorable health result. Safety decisions and medical care must not be conditioned on producing a preferred dataset.
Explain what stopping means.
The study must explain how to stop future collection and request changes or deletion where applicable. It must distinguish data still held by LifeFrom, records already delivered under contract and material already used in training.
Do not promise that every downstream model can be untrained. Explain practical and legal limits before permission is obtained, with recipient obligations and a process for handling requests.