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Clinical Trials/NCT05997771
NCT05997771
Completed
Not Applicable

A Personal Nutrition Advisor to Assist Remote Dietary Counselling for Weight Loss and Maintenance

Lia Bally1 site in 1 country81 target enrollmentAugust 25, 2023
ConditionsObesity

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obesity
Sponsor
Lia Bally
Enrollment
81
Locations
1
Primary Endpoint
The overall mean score of the "perceived impact" section from the user version of the mobile application scale (uMARS )
Status
Completed
Last Updated
last year

Overview

Brief Summary

The purpose of the study is to assess the usability of the PNA and satisfaction with the treatment within the framework of usual care remote nutritional counselling for GLP-1-supported weight management and collect pilot data on its potential to support weight loss.

Detailed Description

The global prevalence of obesity and overweight is increasing and persistently drives global mortality and morbidity.As overweight and obesity are the result of an imbalance between energy intake and energy use, achieving a negative energy balance build the foundation for weight loss. Whilst dietary modification as a standalone procedure often fail in achieving or maintaining weight loss, the recent advent of supportive Glucagon-like Peptide-1 (GLP-1) based pharmacotherapies have greatly changed the landscape.Dietary counselling help people on GLP-1 based treatment reaching their individual weight goals and continued reimbursement of medication costs. However, nutritional advice provided by dietitians is often generic, not sufficiently aligned to individual weight loss trajectories. The "Personal Nutrition Advisor" (PNA) is a decision support tool which is built upon an interpretable weight prediction model based on the energy balance equation (energy intake is a function of recorded dietary intake and a latent part dependent on observed weight changes, whereas energy expenditure is a function of weight and physical activity). Food, weight- and activity records captured using a smartphone application represent input data to the model. Output of the model is the predicted body weight trajectory alongside with personalized recommendations to reach a pre-defined target weight. Integrating the PNA into a remote dietary counselling programme, in which certified dietitians deliver nutritional and lifestyle coaching via an application, has the potential to improve treatment satisfaction and efficacy. Therefore, the purpose of the study assess the usability of the PNA and satisfaction with the treatment within the framework of usual care remote nutritional counselling for GLP-1-supported weight management and collect pilot data on its potential to support weight loss.

Registry
clinicaltrials.gov
Start Date
August 25, 2023
End Date
May 6, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Lia Bally
Responsible Party
Sponsor Investigator
Principal Investigator

Lia Bally

Prof. Dr.med. et Dr. phil.

Insel Gruppe AG, University Hospital Bern

Eligibility Criteria

Inclusion Criteria

  • Written informed consent
  • Receiving GLP-1-based pharmacotherapy in combination with remote nutritional counselling
  • Achieved weight loss of ≥5 (for baseline BMI 28-35 kg/m2) or ≥7% (for baseline BMI≥35kg/m2) after 4 months of GLP-1 based therapy (1st milestone)

Exclusion Criteria

  • Inability to give written informed consent
  • Any physical or psychological disease or condition likely to interfere with the normal conduct of the study and interpretation of the study results
  • Self-reported pregnancy, planed pregnancy within next 3 months or breast-feeding
  • Concomitant participation in another trial that interferes with the normal conduct of the study and interpretation of the study results
  • Not proficient in German

Outcomes

Primary Outcomes

The overall mean score of the "perceived impact" section from the user version of the mobile application scale (uMARS )

Time Frame: Post intervention visit (3 months after baseline)

This outcome will evaluate patient satisfaction with the counselling of the "Personal Nutrition Advisor" (PNA) -assisted remote nutritional counselling. The uMARS includes a 5 point likert scale of agreement (5 points=strongly agree, 1 point= strongly disagree) of 5 questions.

Change in the overall mean satisfaction score of the Nutritional and Dietetic Patient Outcomes Questionnaire (NDPOQ)

Time Frame: From baseline to 3 months of the respective study period

This outcome will evaluate the patient treatment satisfaction with the counselling of the "Personal Nutrition Advisor" (PNA) -assisted remote nutritional counselling. The NDPOQ includes a 5 point likert scale of agreement (5 points=strongly agree, 1 point= strongly disagree) of 15 questions.

The overall mean score of the Healthcare Systems Usability Scale (HSUS)

Time Frame: Post intervention visit (3 months after baseline)

This outcome will evaluate dietitian reported usability of the "Personal Nutrition Advisor" (PNA)- assisted remote nutritional counselling. HSUS includes a 5 point likert scale of agreement (5 points=strongly agree, 1 point= strongly disagree) of 20 questions.

Secondary Outcomes

  • Proportion of patients reaching >5% weight loss(At start of the GLP-1 based pharmacotherapy to 3 months of the respective study period)
  • Change in energy expenditure (kcal/day)(From the first day of the respective study period to 3 months thereafter)
  • Collection of open ended PNA specific feedback questionnaires(Post intervention visit (3 months after baseline))
  • Proportion of patients reaching >15% weight loss(At start of the GLP-1 based pharmacotherapy to 3 months of the respective study period)
  • Change in daily number of logged meals and beverages(From the first day of the respective study period to 3 months thereafter)
  • Change in relative fiber content (%)(From the first day of the respective study period to 3 months thereafter)
  • Change in self-reported exercise engagement per week (hours/week)(At baseline and at 3 months of study intervention)
  • Change in the overall mean score of the General Self-efficacy Scale (GSE) from Imperial College London(From baseline to 3 months of the respective study period)
  • Change in self reported weight (%)(From baseline to 3 months of the respective study period)
  • Change in energy intake (kcal/day)(From the first day of the respective study period to 3 months thereafter)
  • Change in relative protein content (%)(From the first day of the respective study period to 3 months thereafter)
  • Change in relative fat content (%)(From the first day of the respective study period to 3 months thereafter)
  • Change in relative carbohydrate content (%)(From the first day of the respective study period to 3 months thereafter)
  • Proportion of patients reaching >10% weight loss(At start of the GLP-1 based pharmacotherapy to 3 months of the respective study period)
  • Qualitative collection of patient reported PNA specific feedback.(Post intervention visit (3 months after baseline))

Study Sites (1)

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