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Implications of Self-weighing During Weight Loss Treatment

Implications of Self-weighing During Weight Loss Treatment: A Pragmatic 6-month Randomized Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04032249
Enrollment
70
Registered
2019-07-25
Start date
2018-02-01
Completion date
2020-06-01
Last updated
2019-07-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Behavior, Eating, Overweight and Obesity, Signs and Symptoms

Keywords

Obesity, Self-weighing, Weight loss, Mobile health

Brief summary

This study aims to analyze the effectiveness of introducing behavioral elements in a weight loss program, in this case, comparing the difference between self-weighing versus not doing so.

Interventions

BEHAVIORALControl Group (CG)

The control group is subjected to follow a hypocaloric diet and receives information about the benefits of having healthy habits in relation to decision making and food

The control group is subjected to follow a hypocaloric diet and receives information about the benefits of having healthy habits in relation to decision making and food, but also, they will have monitored the self-control of the weight in order to compare the impact of self-weighing versus not doing it

Sponsors

Universidad de Córdoba
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
MALE
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Having a IMC \>25, * Being sedentary and * Have not been submitted to a restrictive diet in the 6 months preceding this study

Exclusion criteria

* Suffered from type 2 diabetes or renal conditions * Being pregnancy or attempt at pregnancy, * Undergoing antidepressant pharmacological treatment

Design outcomes

Primary

MeasureTime frameDescription
Changes from baseline BMIAt baseline (0 years) and followed for 2 yearsBaseline mean BMI values will be measured and compared at 3, 6, 12 and 24 months. BMI will be assessed on a monthly basis during nutritional consultation through a Bioelectrical Impedance Analysis method using a Tanita BC-418 Segmental Body Composition Analyser/Scale
Changes from baseline Fatty massAt baseline (0 years) and followed for 2 yearsBaseline mean Fatty mass values will be measured and compared at 3, 6, 12 and 24 months. Fatty mass will be assessed on a monthly basis during nutritional consultation through a Bioelectrical Impedance Analysis method using a Tanita BC-418 Segmental Body Composition Analyser/Scale. Fatty mass is measured as a percentage.
Changes from baseline Free-fatty massAt baseline (0 years) and followed for 2 yearsBaseline mean Free-fatty mass values will be measured and compared at 3, 6, 12 and 24 months. Free-fatty mass will be assessed on a monthly basis during nutritional consultation through a Bioelectrical Impedance Analysis method using a Tanita BC-418 Segmental Body Composition Analyser/Scale. Fatty mass is measured as a percentage.
Changes from baseline Muscular MassAt baseline (0 years) and followed for 2 yearsBaseline mean Muscular Mass values will be measured and compared at 3, 6, 12 and 24 months. Muscular Mass will be assessed on a monthly basis during nutritional consultation through a Bioelectrical Impedance Analysis method using a Tanita BC-418 Segmental Body Composition Analyser/Scale. Fatty mass is measured as a Kg.
Changes from baseline Corporal WaterAt baseline (0 years) and followed for 2 yearsBaseline mean Corporal Water values will be measured and compared at 3, 6, 12 and 24 months. Corporal Water will be assessed on a monthly basis during nutritional consultation through a Bioelectrical Impedance Analysis method using a Tanita BC-418 Segmental Body Composition Analyser/Scale. Fatty mass is measured as a Kg.
Adherence to dietary pattern will be also measured through personal interviewAt baseline (0 years) and followed for 2 yearsParticipants will be subjected for an intervention based on nutritional (control group) and physical education (two intervention arms) during 24 months. Partial measures will be also taken every week. In the end of the trial, changes in dietary patterns will be measured comparing means differences between baselines, 3, 6, 12 and 24 months.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026