Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07183228

Eatit's Multimodal Digital Lifestyle Intervention for Obesity: A Clinical Pilot Study on Effects on Weight, Self-Rated Eating Habits and Self-Rated Health

Led by Eatit AB · Updated on 2025-09-19

93

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

E

Eatit AB

Lead Sponsor

S

Sahlgrenska University Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

Obesity is a growing public health issue in Sweden with uneven access to care depending on location. Researchers are evaluating Eatit's multimodal digitally dietitian-supported lifestyle intervention to see how it affects weight loss, eating habits, and self-rated health in adults with obesity. This pilot study aims to document the clinical effects of this accessible treatment alternative over six months. Participants use the Eatit app for six months, starting with a core program of 11 weekly modules featuring weekly video consultations and messaging with a licensed dietitian. After completing this phase, monthly video consultations continue, focusing on helpful skills or physical activity support. The program combines behavior change techniques with personalized nutrition counseling. Throughout the study, participants record their weight and waist circumference weekly in the app and complete questionnaires on eating habits and health at the start, three months, and six months. Data collected include demographics, program usage, and self-assessments. The main outcome is change in body weight after six months, with secondary outcomes including waist size and self-rated health improvements. The study lasts six months with ongoing dietitian support and data analysis planned.

CONDITIONS

Brief Title

Eatit's Obesity Intervention: Effects on Weight, Eating Habits and Health

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Body mass index (BMI) of 30 or higher
  • BMI between 27 and 30 with at least one of: obesity diagnosis from another healthcare provider, a related comorbidity, central obesity (waist >80 cm for women or >94 cm for men), or a low Kostindex score indicating risk of rapid weight gain
  • Ability to read and understand Swedish
  • Not currently using or planning to use appetite-suppressing medication
  • Not pregnant
  • Patients with BMI over 40 may be included if no contraindications exist and dietitian assessment allows
Not Eligible

You will not qualify if you...

  • BMI less than 27
  • Medical conditions where weight change may worsen disease (e.g., cancer, COPD)
  • Extensive comorbidities requiring more care than the program provides
  • Untreated depression or eating disorders requiring specialized care
  • Severe psychiatric illness without ongoing support
  • Ongoing substance abuse
  • Suicidal behavior or self-harm in the past six months
  • Conditions requiring individual assessment that may affect treatment outcomes
  • Symptoms of binge eating without full disorder diagnosis unless willing to engage with program
  • Psychiatric disorders under care needing evaluation for program suitability
  • Neuropsychiatric disorders without sufficient concentration or planning ability
  • Severe sleep problems that impair engagement with treatment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

2 video assessment visits for eligibility and informed consent

Outpatient Treatment

Duration - 6 months

Participants engage in a multimodal digital lifestyle intervention for obesity with dietitian support via chat and video.

Weekly dietitian support via video and messaging for 11 weeks, followed by monthly video consultations up to six months

Trial Site Locations

Total: 1 location

1

Eatit AB

Stockholm, Stockholm County, Sweden, 120 30

Actively Recruiting

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Research Team

A

Agnes C Thiel, MSc in Psychology

M

Moa Olson, B.Sc.in Dietetics

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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Frequently Asked Questions

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