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Not yet recruitingNCT07869784Updated Oct 13, 2026

Guided Physical Activity Counseling: A Pilot Study

An interventional study of Physical Activity Counseling Tool (PACT) in Physical Activity, Fitness Tracker and Behavioral Intervention, sponsored by University of California, San Diego. Not yet recruiting at 1 site in United States. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-10-13.

Sponsored by University of California, San Diego · Not applicable, Interventional, and Prevention

Updated Oct 13, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
46
Allocation
Not applicable
Ages
18 Years to 80 Years
Sex
All
01

Study summary

This 1-arm pilot study will test the feasibility of recruitment and use of the Physical Activity Counseling Tool (PACT) in 40 UC San Diego Health patients.

Read the detailed description

The purpose of this study is to pilot test the use of physical activity summary reports and counseling guides for healthcare providers based on continuous objective activity data from wearable fitness trackers, and to test the potential effectiveness and usability of the system in counseling patients. The proposed strategy will leverage existing technologies while addressing barriers to incorporating them into clinical care, and will have high potential for broad reach, low-cost implementation across clinical settings.

02

Conditions studied

  • Physical Activity
  • Fitness Tracker
  • Behavioral Intervention
  • Primary Care

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Keywords

  • physical activity
  • fitness tracker
  • behavioral intervention
  • physical activity counseling
  • exercise
03

In context

Motor Activity

2,646 studies on the registry are indexed under Motor Activity; 1,205 are open to participants now.

This study's planned enrollment of 46 is below the median of 60 across 2,309 interventional studies indexed under Motor Activity.

Browse Motor Activity studies →

Lead sponsor

University of California, San Diego is the lead sponsor of 975 studies on the registry; 196 are open to participants now.

Of its 111 completed or terminated interventional studies of FDA-regulated products, 71 (64%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Providers will be eligible if they:

-currently work for UC San Diego Health

Patients will be eligible if:

  • they are receiving care from one of the enrolled providers;
  • their enrolled provider thinks they can engage in unsupervised physical activity; -they are engaging in \<150 minutes/week of moderate intensity exercise;
  • they are between 18 and 80 years old;
  • they have a smartphone or tablet compatible with the Fitbit app

Exclusion criteria

Exclusion Criteria:

Providers will be excluded if they:

-are planning to leave UCSD in the next 12 months

Patients will be excluded if they:

  • have any condition that would contraindicate unsupervised exercise as determined by their provider
  • plan to change healthcare providers within the next 2 months
  • have a planned surgery or procedure that could impact mobility within the next 3 months;
  • are pregnant
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
46 participants (estimated)

Study arms

  • Experimental
    Physical Activity Counseling Tool (PACT)

    The primary goal of PACT is to use patients' Fitbit data to support provider discussions about physical activity, encourage goal setting, and promote increased physical activity for prevention.

    Behavioral: Physical Activity Counseling Tool (PACT)

Interventions

  • BehavioralPhysical Activity Counseling Tool (PACT)

    PACT aims to use Fitbit data to support patient-provider discussions, goal setting, and increased physical activity for prevention.

06

What researchers measure

Primary outcomes

  1. Participant Enrollment (Persons)

    Enrolling 40 UCSD patients to assess feasibility in recruiting patients and provider use of the PACE tool.

    Time frame: 1 year

  2. Patient After-Visit Questionnaire

    A questionnaire for patients following their provider visit to evaluate the extent to which the physical activity counseling tool was utilized and how satisfied patients were with the discussion.

    Time frame: 6 weeks

  3. Provider Satisfaction Survey

    A questionnaire measuring the provider's satisfaction with the physical activity counseling tool, including its ease of use and perceived effectiveness/usefulness at guiding a physical activity counseling discussion with patients.

    Time frame: 1 year

  4. Weekly MVPA minutes

    Measuring patients' change in MVPA minutes using Fitbit activity tracker

    Time frame: 3 months

07

Study locations

1 site
  • University of California, San Diego
    La Jolla, California 92093, United States
    • Britta Larsen, PhD · Contact · blarsen@health.ucsd.edu · 858-534-8429
    • Britta Larsen, PhD · Principal investigator
    • Sheri Hartman, PhD · Principal investigator
08

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 13, 2026
Show all 1 update
  1. Oct 13, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07869784
Responsible party
Britta Larsen (Associate Professor, University of California, San Diego) — Principal investigator
First posted
Oct 13, 2026
Start date
Jan 15, 2027 (estimated)
Primary completion
Oct 15, 2027 (estimated)
Completion
Jan 15, 2028 (estimated)
Last update
Oct 13, 2026

Study contacts

Britta Larsen, PhD
Contact
blarsen@health.ucsd.edu
858-534-8429

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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