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RecruitingNCT06570642Updated Jun 27, 2025

eMOTION: Examining Affective Mechanisms in Physical Activity Engagement

An interventional study of Physical Activity Goals mHealth Intervention and TYPE/CONTEXT enhancement in Physical Inactivity, Overweight or Obesity and Cancer, sponsored by University of Southern California. Recruiting at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-06-27.

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

From the registry’s dates

  • Started Aug 2024; still recruiting 2 years 1 month later.
Phase
Not applicable
Study type
Interventional
Enrollment
280
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

This early-phase trial will test intervention strategies to influence affective mechanisms underlying physical activity and determine whether changes in those mechanisms result in change in physical activity behavior among inactive adults who are overweight or obese.

Read the detailed description

This ORBIT model phase 1 trial will examine whether affective mechanisms (1) can be experimentally manipulated in real-world settings; and (2) mediate the relationship between interventions and physical activity behavior. A novel physical activity intervention will be optimized by efficiently disentangling the effects of its core component and two enhancement components on affective mechanisms associated with physical activity engagement.

02

Conditions studied

  • Physical Inactivity
  • Overweight or Obesity
  • Cancer

Keywords

  • Affective Response
  • Psychological Needs
  • Physical Activity
03

In context

Sedentary Behavior

332 studies on the registry are indexed under Sedentary Behavior; 155 are open to participants now.

This study's planned enrollment of 280 is above the median of 70 across 287 interventional studies indexed under Sedentary Behavior.

Browse Sedentary Behavior studies →

Lead sponsor

University of Southern California is the lead sponsor of 773 studies on the registry; 135 are open to participants now.

Of its 68 completed or terminated interventional studies of FDA-regulated products, 32 (47%) have results posted.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  1. Aged ≥ 18 years
  2. Reside in the United States
  3. Self-reported BMI ≥ 25
  4. Current structured physical activity engagement \< 60 minutes per week
  5. Own a personal smartphone device
  6. Reside in an area with Internet or Wi-Fi connectivity during the study period
  7. Able to speak and read in English
  8. Interested and willing to start a physical activity program
  9. 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 previously worn, for the duration of the study period
  10. 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

Exclusion criteria

Exclusion Criteria:

  1. Inability to provide informed consent due to cognitive disability
  2. Inability 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 or answer brief surveys on the smartwatch for any reason
  3. Current pregnancy
  4. Referred to the study by another participant or from Reddit.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Factorial assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
280 participants (estimated)

Study arms

  • Experimental
    Affect (no enhancements) > Intensity

    Participants receive affect-based goals for the first 8-weeks, then cross-over to receive intensity-based goals for the second 8-weeks. No enhancements are added to the standard mHealth intervention.

    Behavioral: Physical Activity Goals mHealth Intervention

  • Experimental
    Intensity > Affect (no enhancements)

    Participants receive intensity-based goals for the first 8-weeks, then cross-over to receive affect-based goals for the second 8-weeks. No enhancements are added to the standard mHealth intervention.

    Behavioral: Physical Activity Goals mHealth Intervention

  • Active comparator
    Affect (+ SAVOR + TYPE/CONTEXT) > Intensity

    Participants receive affect-based goals for the first 8-weeks. In addition to the standard mHealth intervention, participants engage in both SAVOR and TYPE/CONTEXT enhancements to augment the treatment effects of the affect-based goals condition. Participants then cross-over to receive intensity-based goals for the second 8-weeks.

    Behavioral: Physical Activity Goals mHealth Intervention · Behavioral: TYPE/CONTEXT enhancement · Behavioral: SAVOR enhancement

  • Active comparator
    Intensity > Affect (+ SAVOR + TYPE/CONTEXT)

    Participants receive intensity-based goals for the first 8-weeks, then cross-over to receive affect-based goals for the second 8-weeks. In addition to the standard mHealth intervention, participants engage in both SAVOR and TYPE/CONTEXT enhancements to augment the treatment effects of the affect-based goals condition.

    Behavioral: Physical Activity Goals mHealth Intervention · Behavioral: TYPE/CONTEXT enhancement · Behavioral: SAVOR enhancement

  • Active comparator
    Affect (+SAVOR) > Intensity

    Participants receive affect-based goals for the first 8-weeks. In addition to the standard mHealth intervention, participants engage in the SAVOR enhancement to augment the treatment effects of the affect-based goals condition. Participants then cross-over to receive intensity-based goals for the second 8-weeks.

    Behavioral: Physical Activity Goals mHealth Intervention · Behavioral: SAVOR enhancement

  • Active comparator
    Intensity > Affect (+SAVOR)

    Participants receive intensity-based goals for the first 8-weeks, then cross-over to receive affect-based goals for the second 8-weeks. In addition to the standard mHealth intervention, participants engage in the SAVOR enhancement to augment the treatment effects of the affect-based goals condition.

    Behavioral: Physical Activity Goals mHealth Intervention · Behavioral: SAVOR enhancement

  • Active comparator
    Affect (+TYPE/CONTEXT) > Intensity

    Participants receive affect-based goals for the first 8-weeks. In addition to the standard mHealth intervention, participants engage in the TYPE/CONTEXT enhancement to augment the treatment effects of the affect-based goals condition. Participants then cross-over to receive intensity-based goals for the second 8-weeks.

    Behavioral: Physical Activity Goals mHealth Intervention · Behavioral: TYPE/CONTEXT enhancement

  • Active comparator
    Intensity > Affect (+TYPE/CONTEXT)

    Participants receive intensity-based goals for the first 8-weeks, then cross-over to receive affect-based goals for the second 8-weeks. In addition to the standard mHealth intervention, participants engage in the TYPE/CONTEXT enhancement to augment the treatment effects of the affect-based goals condition.

    Behavioral: Physical Activity Goals mHealth Intervention · Behavioral: TYPE/CONTEXT enhancement

Interventions

  • BehavioralPhysical Activity Goals mHealth Intervention

    On days participants plan to exercise, they engage in two daily goal sessions (morning and evening). Morning sessions provide an activity goal for the day and ask the participant to create a plan, anticipate barriers, and brainstorm solutions for achieving this goal. The affect-based goal condition asks participants to engage in either (1) a type (50% of daily goals) or (2) a context (50% of daily goals) of physical activity that allows them to experience positive affect. Goals focused on context are randomly generated to suggest that the participant performs activity (1) in a place; (2) in a social situation; or (3) while listening to something that makes them feel good. The intensity-based goal condition asks participants to maintain a certain target heart rate range during physical activity. Starting heart rate reflects the approximate age-adjusted heart rate max, with goals progressively increasing from 55% to 70% heart rate max.

  • BehavioralTYPE/CONTEXT enhancement

    TYPE/CONTEXT augments intervention effects by providing tailored recommendations for activity types and contexts that satisfy personally-important psychological needs as rated by each participant at baseline. Ratings from a crowdsourced panel of adults on Amazon Mechanical Turk will be used to determine the potential for specific activity types and contexts to satisfy psychological needs; our tailoring algorithm will then recommend the corresponding activity type or context while accounting for reported constraints (e.g., ability, access). These details will be incorporated into a tailored recommendation provided to participants each Sunday as they make activity plans for the upcoming week. Specifically, the program will randomly select either type or context (i.e., location, audio, social) recommendations and will rotate every two weeks. For TYPE, participants' top 3 activity types are recommended; for CONTEXT, participants' top 3 activity contexts are recommended.

  • BehavioralSAVOR enhancement

    SAVOR implements a brief savoring exercise on the smartphone that takes place either after the planned physical activity session or during the evening goal session (after the self-monitoring module). Participants will respond to questions that are intended to enhance and prolong positive experiences during physical activity. To trigger attentional deployment, a common savoring strategy that involves intensifying experiences by focusing on them, participants will answer three open-ended prompts. These prompts are drawn from a prompt pool with slightly varied wording to promote a sense of novelty. Savoring prompts will rotate daily and have a day lag built in every week (i.e., Week 1 Monday Savoring Prompts are Week 2 Tuesday Savoring Prompts).

06

What researchers measure

Primary outcomes

  1. Physical Activity: Step Count

    Daily steps will be calculated from minute-level accelerometer data. Fitbit Versa 3 smartwatches with internal accelerometers are worn for the duration of the study period, except while bathing or charging. Only days with sufficient wear time (defined as ≥ 10-hours of valid data, where no more than 20-minutes per hour has a consecutive step count of zero) are used for analysis.

    Time frame: Daily total for weeks 1-19

  2. Physical Activity: Minutes

    Daily minutes of light, moderate, and vigorous physical activity will be calculated from minute-level accelerometer data. Fitbit Versa 3 smartwatches with internal accelerometers are worn for the duration of the study period, except while bathing or charging. Only days with sufficient wear time (defined as ≥ 10-hours of valid data, where no more than 20-minutes per hour has a consecutive step count of zero) are used for analysis.

    Time frame: Daily total for weeks 1-19

Secondary outcomes

  1. Affective Response

    Event-contingent ecological momentary assessment (EMA) check-ins sent to the smartwatch during physical activity measure affective response. Event-contingent EMA are triggered when Fitbit sensors detect physical activity via moving average heart rate. A ≥30-minute buffer separates the first and second EMA during a single physical activity bout. A maximum of two event-contingent EMA will be sent within any given 60-minute period. Participants are asked to safely pause their activity to answer seven items about their affective response using a 5-point bipolar Likert Scale. Five items (Energetic-Fatigued, Happy-Discouraged, Relaxed-Tense, Excited-Bored, Satisfied-Frustrated) are drawn from Russell's Circumplex Model of Affect; one (Good-Bad) represents core affective valence; and one (Proud-Embarrassed) represents self-conscious emotion.

    Time frame: Max 2 per 60-min physical activity period during weeks 2-9 and weeks 12-19

  2. Affectively-Charged Motivations

    Affectively-charged motivations for physical activity are measured during the morning goal session via REDCap. A text message alerts participants to complete the morning goal session on their smartphone. A single item from the Attraction-Antipathy subscale of the AFFEXX measures affectively-charged motivation by asking, "How do you feel about doing physical activity today?". Participants select a response using a Visual Analogue Scale ranging from 0 (Dread) to 100 (Excited).

    Time frame: Up to once daily for weeks 2-9 and weeks 12-19

  3. Anticipated Affect

    Anticipated affect is measured during the morning goal session via REDCap. A text message alerts participants to complete the morning goal session on their smartphone. A single item asks, "How do you expect to feel during physical activity today?". Participants select a response using a Visual Analogue Scale ranging from 0 (Miserable) to 100 (Thrilled).

    Time frame: Up to once daily for weeks 2-9 and weeks 12-19

07

Study locations

1 of 1 sites recruiting
  • University of Southern California
    Los Angeles, California 90032, United States
    Recruiting
08

References and documents

Publications

  • Dunton GF, Hatzinger L, Crosley-Lyons R, Hewus M, Wang WL, Van Dyck D, Huh J. Randomized trial of a digital therapeutics intervention to enhance affective response during physical activity: Protocol for the eMOTION study. Contemp Clin Trials. 2025 Jul;154:107945. doi: 10.1016/j.cct.2025.107945. Epub 2025 May 12. PubMed 40368026 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 27, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06570642
Lead sponsor
University of Southern California
Collaborators
National Cancer Institute (NCI)
Responsible party
Genevieve Dunton (Chief, Division of Health Behavior Research and Director, USC Real-Time Eating Activity and Children's Health (REACH) Lab, University of Southern California) — Principal investigator
First posted
Aug 26, 2024
Start date
Aug 14, 2024
Primary completion
Jan 1, 2027 (estimated)
Completion
Jun 30, 2027 (estimated)
Last update
Jun 27, 2025

Study contacts

Micaela Hewus, MPH
Contact
micaelag@usc.edu
323-442-7304
Rachel C Lyons, MS
Contact
rclyons@usc.edu
3175187670
Genevieve F Dunton, PhD MPH
principal investigator · University of Southern California

Oversight

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

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