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Overweight or ObesityMomentumNCT07708064

Testing Just-in-Time Adaptive Interventions (JITAIs) to Prevent Goal Disengagement in Response to Weight Regain

A study testing JITAI Combined with psychological intervention in people with Overweight or Obesity, run by ORI Community and Evaluation Services at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This trial will test the effectiveness of a weight loss maintenance intervention designed to help participants respond more adaptively to weight regain. Participants will be randomly assigned to one of two conditions. Read more about this study

Who is it for?
Ages 18 to 70 years
Conditions the study is for
Overweight or Obesity
What is being tested?
JITAI Combined with psychological intervention
Could I receive a placebo?
No, everyone receives an active treatment
How many people
120 participants
Where
1 siteUnited States
Study dates
14 Jul 2026to 31 Dec 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 70 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Ages 18-70 years
  • BMI of 25-50 kg/m2
  • Current weight is 3% lower than their highest weight in the past 3 years
  • Desire to maintain their weight or lose more
  • Ability to engage in PA, as defined as being able to walk two full city blocks without stopping
  • Smartphone and Internet access
  • Successful completion of all enrollment procedures
  • Ability to attend a workshop(s) on a Monday or Tuesday evening

Who cannot join

  • History of bariatric surgery
  • History of being diagnosed with an eating disorder
  • Currently pregnant, breastfeeding, or planning to become pregnant in the next 24 months
  • Enrolled in another formal weight loss/weight maintenance program
  • Currently taking a GLP-1 medication.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Charlotte Hagerman, PhD contact

14109372035

chagerman@ori.org

United States1 site, 1 recruiting
  • Oregon Research Institute Community and Evaluation Services

    Springfield, Oregon, 97477

    Charlotte Hagerman, PhD, 4109372035, chagerman@ori.org

    Recruiting

Other trials in United States

About this study

This trial will test the effectiveness of a weight loss maintenance intervention designed to help participants respond more adaptively to weight regain. Participants will be randomly assigned to one of two conditions. In one condition, participants will receive brief exercises (e.g., written reflections, videos) sent to through a smartphone app immediately after they regain weight or miss a weigh-in. These exercises will use mindfulness, acceptance, and self-compassion strategies to help participants stay motivated for their long term goals, even when weight regain feels demoralizing. In the comparison condition, participants will receive weekly reminders of standard weight control strategies strategies.

Being tested
JITAI Combined with psychological intervention, Active Control
Keywords
just-in-time adaptive interventions, weight regain, self-weighing, self-compassion, acceptance-based behavioral treatments, mindfulness, behavioral weight loss
Medical subject headings
Overweight, Obesity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • JITAI Combined with psychological interventionBehavioural

    For six months, participants will receive a just-in-time adaptive interventions via a smartphone app immediately after they gain weight or they skip a weigh-in (according to a specific algorithm). Interventions will engage participants in mindfulness, acceptance, and self-compassion-based (MASC) strategies through different modalities (e.g., writing exercises, videos, audio reflections). They will take approximately 1-10 minutes. Participants will also attend an introductory workshop, during which they will receive the instructions weigh daily, learn the importance of quickly responding to weight regain, and be introduced to MASC strategies. They will also attend two booster workshops during the 6-month period.

  • Active ControlBehavioural

    For six months, participants will receive weekly, automated messages via a smartphone app with reminders of standard behavioral weight control principles. Participants will attend an introductory workshop, during which they will receive instructions to weigh daily and learn the importance of responding to weight regain.

Study groups in NCT07708064
Study groupRoleWhat they receive
JITAI ConditionExperimentalParticipants in this condition will receive a 6-month weight loss maintenance intervention that uses mindfulness, acceptance, and self-compassion strategies to respond to weight regain.
Receives: Behavioral: JITAI Combined with psychological intervention
Active Control ConditionActive comparatorParticipants in this condition will receive minimal intervention designed to reflect "usual care" for weight loss maintenance.
Receives: Behavioral: Active Control

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. State negative affect

    Through ecological assessment surveys, participants will respond to a single item measuring their current negative affect.

    Measured: Whenever participants skip a weigh-in or regain weight during the 6 month study period

  2. State shame

    Through ecological assessment surveys, participants will respond to a single item measuring their current shame.

    Measured: Whenever participants skip a weigh-in or regain weight during the 6 month study period

  3. State Motivation

    Through ecological assessment surveys, participants will respond to a single item measuring their current feelings of motivation.

    Measured: Whenever participants skip a weigh-in or regain weight during the 6 month study period

  4. State Self-Efficacy

    Through ecological assessment surveys, participants will respond to a single item measuring their current self-efficacy.

    Measured: Whenever participants skip a weigh-in or regain weight during the 6 month study period

  5. Current confidence in the effectiveness of weight control behaviors

    Through ecological assessment surveys, participants will respond to a single item measuring their current confidence in the effectiveness of weight control behaviors.

    Measured: Whenever participants skip a weigh-in or regain weight during the 6 month study period

  6. State self-compassion

    Through ecological assessment surveys, participants will respond to a single item measuring their state self-compassion.

    Measured: Whenever participants skip a weigh-in or regain weight during the 6 month study period

  7. State mindfulness

    Through ecological assessment surveys, participants will respond to a single item measuring their state mindfulness.

    Measured: Whenever participants skip a weigh-in or regain weight during the 6 month study period

  8. State acceptance

    Through ecological assessment surveys, participants will respond to a single item measuring their state acceptance.

    Measured: Whenever participants skip a weigh-in or regain weight during the 6 month study period

  9. Self-serving interpretation of weight gain

    Through ecological assessment surveys, participants will respond to a single item measuring their self-serving interpretation of the weight regain.

    Measured: Whenever participants regain weight during the 6 month study period

  10. Daily Calorie Tracking (Yes/No)

    Whether participants log their calories (at least 800 calories) using a dietary tracking app that day (yes/no).

    Measured: Whenever participants skip a weigh-in or regain weight during the 6 month study period

  11. Daily MVPA

    Minutes of moderate-to-vigorous physical activity they engage in that day, as tracked by their Fitbit band.

    Measured: Whenever participants skip a weigh-in or regain weight during the 6 month study period

  12. Likelihood of weighing in the following day

    Likelihood that participants weigh themselves the following day on a wireless smart scale (yes/no).

    Measured: Whenever participants skip a weigh-in or regain weight during the 6 month study period

  13. Weight change

    Using participants' weights from a wireless scale, their percent weight change from the beginning to the end of the study period will be calculated.

    Measured: End of treatment (6 months after baseline)

  14. Intervention acceptability

    Intervention acceptability will be operationalized as the percent of participants who indicate that they are "satisfied" or "very satisfied" with the program on an anonymous survey that they complete during their individual interview.

    Measured: End of treatment (6 months after baseline)

  15. Calorie Tracking Frequency

    The number of days that participants logged their calories (at least 800 calories) using a dietary tracking app during the study period.

    Measured: 6 months (duration of study period)

  16. Average Weekly MVPA

    Average total minutes of weekly moderate-to-vigorous physical activity, as tracked by their Fitbit band, during the study period.

    Measured: 6 months (duration of study period)

  17. Frequency of Weighing In

    Total number of days that participants weighed themselves on a wireless smart scale during the study period.

    Measured: 6 months (duration of study period)

Secondary outcomes (3)
  1. Mindfulness (Hypothesized intervention mediator)

    Participants will self-report their mindfulness using the Awareness subscale of The Philadelphia Mindfulness Scale. The range of scores is 1-5, with higher scores indicating greater mindfulness.

    Measured: Mid-Treatment (3 months after baseline)

  2. Acceptance (Hypothesized intervention mediator)

    Participants will self-report their mindful acceptance using the Acceptance subscale of The Philadelphia Mindfulness Scale. The range of scores is 1-5, with higher scores indicating greater mindful acceptance.

    Measured: Mid-Treatment (3 months after baseline)

  3. Self-compassion (Hypothesized intervention mediator)

    Participants will report their self-compassion using the Self-Compassion Scale Short Form. Scores can range from 1 to 5, with higher scores indicating higher self-compassion.

    Measured: Mid-Treatment (3 months after baseline)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Jul 2026
  2. Study start14 Jul 2026
  3. Primary completion31 Dec 2027 (estimated)
  4. Study completion31 Dec 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
120 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07708064
Sponsor's protocol ID
K01HL172254
Acronym
Momentum
Status last verified
Aug 2026
First submitted
12 Jul 2026
Last updated
11 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing JITAI Combined with psychological intervention in people with Overweight or Obesity, run by ORI Community and Evaluation Services at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 11 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Charlotte Hagerman, PhD (14109372035, chagerman@ori.org), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

State negative affect (time frame: Whenever participants skip a weigh-in or regain weight during the 6 month study period). The study lists 17 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Aug 2026.

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