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Clinical Trials/NCT06812897
NCT06812897Active, not recruitingNot Applicable

Assessing the Feasibility of a Patient-Driven Chiropractic Patient Portal (SallieTM Life U) for Research Purposes

Life University1 site in 1 country28 target enrollmentStarted: November 1, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Sponsor
Enrollment
28
Locations
1
Primary Endpoint
Participant Recruitment

Study Overview

Brief Summary

This feasibility trial explored the usability of the patient-driven chiropractic patient portal, Sallie™ Life U. The study aimed to recruit 30 participants to track their daily symptoms, triggers, and habits over 30 days while completing three questionnaires about their experience with the portal. The first questionnaire was administered after participants created their accounts, the second at the midpoint of tracking (day 15), and the third upon completing the tracking period (day 30). All participation in the study was conducted remotely using the participants' personal devices.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Have daily access to technology (smartphone, tablet, or computer)
  • •Currently receiving chiropractic care (for the purposes of this feasibility study, this requires at least one chiropractic adjustment each month)

Exclusion Criteria

  • •Given software restrictions, participants must also be able to read and write in English and not be visually impaired.

Outcomes

Primary Outcomes

Participant Recruitment

Time Frame: 30 days

Average # of participants to create a SallieTM Life U account per month

Participant Adherence - Weekly

Time Frame: 30 days

% of participants with daily data input throughout the week

Participant Retention

Time Frame: 30 days

% of participants completing all questionnaires

Participant Adherence - Monthly

Time Frame: 30 days

% of participants with total number of daily data input throughout the month.

Secondary Outcomes

  • Personalized Tracking Metrics (PTMs)(30 days)

Investigators

Sponsor
Life University
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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