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Blue Note Therapeutics Product BNT 103 Usability and User Engagement

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Blue Note Therapeutics

Status

Completed

Conditions

Breast Cancer Female

Treatments

Device: BNT103

Study type

Interventional

Funder types

Industry

Identifiers

NCT05032404
PROT002 - Test Plan 01 Rev A

Details and patient eligibility

About

This test aims to explore product development-focused usability and user engagement.

Full description

Sponsor is testing an innovative peer-to-peer communication tool during this trial.

Enrollment

15 patients

Sex

Female

Ages

35 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient can read, write, and speak in English
  • Patient is between the ages of 35-55
  • Diagnosed with Stage I-III breast cancer
  • In active treatment or within 3 months of ending active treatment and under the care of a clinician at time of study
  • Apple mobile phone or tablet user
  • Willing to participate in study protocol

Exclusion criteria

  • Any participant not meeting inclusion criteria

Trial design

Primary purpose

Device Feasibility

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

15 participants in 1 patient group

BNT103
Experimental group
Description:
All participants receive BNT103. BNT103 provides 10 sessions over approximately 10 weeks.
Treatment:
Device: BNT103

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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