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NCT06125964Completed

eMOTION Formative Study

Using Real-Time Data Capture to Examine Affective Mechanisms as Mediators of Physical Activity Adherence in Interventions: Formative Study

Source: ClinicalTrials.gov · Last updated 14 Aug 2025

Brief summary (registry, in English)

The eMOTION Study is a two-part ORBIT model phase 1 trial. The first part, called the Formative Study, will assess acceptability and feasibility of a novel physical activity intervention in adults at increased risk for cancer due to overweight or obesity.

Status (registry)
Completed
Study type
Interventional
Enrollment
47 (actual)
First submitted
26 Oct 2023
Start date
6 Oct 2023
Primary completion date
30 May 2024
Lead sponsor
University of Southern California
Diseases
Obesity
NCT number
NCT06125964

What you commit to

  • Study type: Interventional
  • Participants enrolled: 47
  • From 6 Oct 2023 to the primary completion date, 30 May 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • unable to engage in one or more key treatment components, including those with medical conditions that preclude physical activity engagement or who cannot wear an accelerometer on the wrist for any reason

Other

  • unable to provide informed consent due to cognitive disability
  • currently pregnant

Who the study is looking for

  • adults aged ≥18 years
  • residing in the United States
  • self-reported BMI ≥ 25
  • currently engaging in \< 60 minutes per week of structured physical activity
  • owning a personal smartphone device
  • residing in an area with Internet or Wi-Fi connectivity during the study period
  • able to speak and read in English
  • interested and willing to start a physical activity program
  • willing to wear a Fitbit Versa smartwatch provided by the study team everyday continuously (including at work and during physical activity), in place of any Fitbits or smartwatches they previously wore, for the duration of the study period
  • able to read the small font on a smartwatch screen without glasses, or willing to carry reading glasses during physical activity for the purpose of reading the smartwatch screen

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
University of Southern California
Coordinator of this site? Confirm its status
Los AngelesUnited StatesUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.