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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05997771
Other study ID # PNA-ORIGINATE
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date August 25, 2023
Est. completion date May 31, 2024

Study information

Verified date February 2024
Source Insel Gruppe AG, University Hospital Bern
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 81
Est. completion date May 31, 2024
Est. primary completion date April 30, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Personal Nutrition Advisor
The study intervention will be the use of the PNA data analysis tool during remote nutritional counselling sessions delivered by certified dietitians, also referred to as PNA-assisted remote nutritional counselling.

Locations

Country Name City State
Switzerland Department of Diabetes, Endocrinology, Clinical Nutrition and Metabolism, Inselspital, Bern University Hospital Bern

Sponsors (1)

Lead Sponsor Collaborator
Lia Bally

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in the overall mean satisfaction score of the Nutritional and Dietetic Patient Outcomes Questionnaire (NDPOQ) 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. From baseline to 3 months of the respective study period
Primary The overall mean score of the "perceived impact" section from the user version of the mobile application scale (uMARS ) 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. Post intervention visit (3 months after baseline)
Primary The overall mean score of the Healthcare Systems Usability Scale (HSUS) 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. Post intervention visit (3 months after baseline)
Secondary Change in self reported weight (%) This outcome will evaluate the potential to support weight loss by PNA-assisted remote nutritional counselling (self-reported weight closest to start and end of the study period). From baseline to 3 months of the respective study period
Secondary Proportion of patients reaching >5% weight loss This outcome will evaluate the potential to support weight loss by PNA-assisted remote nutritional counselling (calculated from the initial weight, measured in-clinic at start of the GLP-1 based pharmacotherapy) At start of the GLP-1 based pharmacotherapy to 3 months of the respective study period
Secondary Proportion of patients reaching >10% weight loss This outcome will evaluate the potential to support weight loss by PNA-assisted remote nutritional counselling (calculated from the initial weight, measured in-clinic at start of the GLP-1 based pharmacotherapy) At start of the GLP-1 based pharmacotherapy to 3 months of the respective study period
Secondary Proportion of patients reaching >15% weight loss This outcome will evaluate the potential to support weight loss by PNA-assisted remote nutritional counselling (calculated from the initial weight, measured in-clinic at start of the GLP-1 based pharmacotherapy) At start of the GLP-1 based pharmacotherapy to 3 months of the respective study period
Secondary Change in daily number of logged meals and beverages This outcome will evaluate the impact of PNA-assisted remote nutritional counselling on frequency of dietary self-monitoring (manual entries of pictures, text tags and food/beverage tags per day) From the first day of the respective study period to 3 months thereafter
Secondary Change in energy intake (kcal/day) This outcome will evaluate the impact of PNA-assisted remote nutritional counselling on PNA derived dietary intake, calculated by the energy balance model embedded in the PNA using manual entries of weight logs, meal logs and activity logs. From the first day of the respective study period to 3 months thereafter
Secondary Change in energy expenditure (kcal/day) This outcome will evaluate the impact of PNA-assisted remote nutritional counselling on PNA derived dietary expenditure, calculated by the energy balance model embedded in the PNA using manual entries of weight logs, meal logs and activity logs. From the first day of the respective study period to 3 months thereafter
Secondary Change in relative carbohydrate content (%) This outcome will evaluate the impact of PNA-assisted remote nutritional counselling on PNA derived nutrient distribution, calculated by the energy balance model embedded in the PNA using manual entries of weight logs, meal logs and activity logs. From the first day of the respective study period to 3 months thereafter
Secondary Change in relative protein content (%) This outcome will evaluate the impact of PNA-assisted remote nutritional counselling on PNA derived nutrient distribution, calculated by the energy balance model embedded in the PNA using manual entries of weight logs, meal logs and activity logs. From the first day of the respective study period to 3 months thereafter
Secondary Change in relative fat content (%) This outcome will evaluate the impact of PNA-assisted remote nutritional counselling on PNA derived nutrient distribution, calculated by the energy balance model embedded in the PNA using manual entries of weight logs, meal logs and activity logs. From the first day of the respective study period to 3 months thereafter
Secondary Change in relative fiber content (%) This outcome will evaluate the impact of PNA-assisted remote nutritional counselling on PNA derived nutrient distribution, calculated by the energy balance model embedded in the PNA using manual entries of weight logs, meal logs and activity logs. From the first day of the respective study period to 3 months thereafter
Secondary Change in self-reported exercise engagement per week (hours/week) This outcome will evaluate the impact of PNA-assisted remote nutritional counselling on self-reported physical activity using manual entries of activity logs. At baseline and at 3 months of study intervention
Secondary Change in the overall mean score of the General Self-efficacy Scale (GSE) from Imperial College London This outcome will evaluate the impact of PNA-assisted remote nutritional counselling on self-efficacy. GSE includes a 5 point Likert scale of confidence (Not at all confident =1 point, Extremely confident=5 points) of 6 questions. From baseline to 3 months of the respective study period
Secondary Collection of open ended PNA specific feedback questionnaires This qualitative outcome will collect opinions from patients and dietitians regarding the components of the PNA with the aim to further optimise its perceived usefulness. Post intervention visit (3 months after baseline)
Secondary Qualitative collection of patient reported PNA specific feedback. This qualitative outcome will be assessed by an semi structured remote patient group interview addressing the patient's perspective on the utility of the dietitians' advice, discrepancy from expectations, general feedback and suggestions for PNA improvement. Post intervention visit (3 months after baseline)
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