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Trial · Observational

Active, not recruitingPhase not statedRegistry data

Does Personality Predict Patient Adherence, Health Behaviors, and Weight Loss Outcomes During the Latino Crossover Semaglutide Study (LCSS)? (Story-LCSS Project)

Short name StoryLCSS

This trial does not test a peptide that PepBank tracks.

  • Measures Semaglutide, does not give it. It appears in an outcome measure.

Overview

Status
Active, not recruiting
Phase
Phase not stated
Enrollment
59 participants (actual)
Sponsor
Loma Linda University · Other
Design
Not stated
Countries
1 country

United States

Start
1 Feb 2023
Primary completion
29 May 2024
Completion
May 2027 (estimated)
First posted
18 Nov 2022
Last update posted
8 Jun 2026
Conditions
Obesity · Body Weight Changes

Timeline

1 trial · 1 ongoing

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
202320242025202620272028
  1. Ph –

    StoryLCSS

    NCT05622045

    1 Feb 2023 to est. May 2027

Registry summary

Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.

The goal of this observational study is to learn about the personality attributes and values of people living with obesity that are part of the Latino community, and how these personality attributes and values can help to predict success during a weight loss program. The main questions it aims to answer are: * What are the personality attributes and values of people living with obesity that sign up to the LCSS-Latino Crossover Semaglutide Study trial? * Can behavioral artificial intelligence (a computer formula) predict which patients will complete the LCSS-Latino Crossover Semaglutide Study trial? * How do behavioral artificial Intelligence predictions (a computer formula) compare to clinician predictions of patient success? * Can behavioral artificial intelligence (a computer formula) predict patient weight loss, calorie consumption and physical activity levels during the LCSS-Latino Crossover Semaglutide Study trial? Participants will be recorded in English and Spanish while responding to a question regarding participation in a weight loss study.

Interventions

  • Voice dataBehavioral

Arms1

  • Other

    Story-LCSS

Primary outcomes4

Outcomes the sponsor listed as primary.

  1. Predicted patient weight change success

    Time frame · The voice data measurement will take place at baseline and take about 10-15 minutes for collection to take place.

    Registry description

    Predicted patient weight change as determined by Scaled Insights Behavioural Artificial Intelligence based on subject voice data. Weight loss exceeding 5-10 pounds over 6 months will be considered to be successful. Predicted weight change will be compared to the weight change measured in a separate clinical trial \[Latino Crossover Semaglutide Study (LCSS) NCT05087342\]. Similar weight change values between the predicted and measured outcomes will indicate that the Scaled Insights Behavioural Artificial Intelligence is good predictor.

  2. Clinician predictions

    Time frame · The clinician judgement will be measured during the second month of the subject's weight loss study.

    Registry description

    Clinician (physician) judgement of patient weight loss success during a weight loss study.

  3. Predicated patient calorie intake

    Time frame · The voice data measurement will take place during the subject's initial clinic visit and take about 10-15 minutes for collection to take place.

    Registry description

    Predicted patient calorie intake as determined by Scaled Insights Behavioural Artificial Intelligence based on subject voice data. Predicted calorie intake will be compared to the calorie intake measured in a separate clinical trial \[Latino Crossover Semaglutide Study (LCSS) NCT05087342\]. Similar calorie values between the predicted and measured outcomes will indicate that the Scaled Insights Behavioural Artificial Intelligence is good predictor.

  4. Predicated patient physical activity level

    Time frame · The voice data measurement will take at baseline and take about 10-15 minutes for collection to take place.

    Registry description

    Predicted patient physical activity level as determined by Scaled Insights Behavioural Artificial Intelligence based on subject voice data. Predicted physical activity will be compared to the physical activity measured in a separate clinical trial \[Latino Crossover Semaglutide Study (LCSS) NCT05087342\]. Similar physical activity level values between the predicted and measured outcomes will indicate that the Scaled Insights Behavioural Artificial Intelligence is good predictor.

Secondary outcomes(2)
  1. Personality attributes and values

    Time frame · The voice data measurement will take place at baseline and take about 10-15 minutes for collection to take place.

    Registry description

    Extrapolated personality attributes and values as determined by Scaled Insights Behavioural Artificial Intelligence based on subject voice data. These are qualitative non-numerical descriptors.

  2. Predicted patient attrition rate

    Time frame · The voice data measurement will take place at baseline and take about 10-15 minutes for collection to take place.

    Registry description

    Predicted patient attrition rate from the weight loss study as determined by Scaled Insights Behavioural Artificial Intelligence based on subject voice data. Predicted patient attrition rate will be compared to the attrition rate occurring during the weight loss study. Similar attrition rates between the predicted and actual rates will indicate that the Scaled Insights Behavioural Artificial Intelligence is good predictor.

Posted results

Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.

No results are posted for this trial.

A trial that is still running, or that stopped early, may post results later.

Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works

Studies1

Studies that cite this trial.

Studies with results

1 study on this page

Indexing hint: Randomized controlled trial · 2021

10 results

Once-Weekly Semaglutide in Adults with Overweight or Obesity.

Wilding et al. 2021The New England journal of medicinecited by 3,862

PMID 33567185DOI 10.1056/nejmoa2032183PUB-33567185

Full text at the publisher10 results

Eligibility

Who could join, as posted.

Sex
All
Age
from 18 Years up to 74 Years
Healthy volunteers
Not stated
Inclusion and exclusion criteria, as posted
Inclusion Criteria: * Participation in the LCSS-Latino Crossover Semaglutide Study Exclusion Criteria: * Not a participant of the LCSS-Latino Crossover Semaglutide Study at the point of data collection

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