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Recruiting

NCT Number: NCT05689762

Promotion of Healthy Lifestyle Habits in Primary Care Settings

Intervention aiming to promote healthy dietary and physical activity behaviors in adults with different socioeconomic status primary care settings

Recruiting

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Key information

Conditions

Healthy Lifestyle

Age range

40 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Örebro University

Örebro, 70182, Sweden

Location status: Recruiting

Location contact

fawzi Kadi, Phd

CONTACT

[email protected]

019302160 ext. 0046

About this study

The project aims to strengthen primary care's ability to promote healthy eating and physical activity habits among population groups with an elevated risk of disease. Participants will receive health counseling focusing of physical activity and diet and will also have access to a digital platform supporting the adoption of healthy lifestyles. The goals of the project are to (1) implement changes and evaluate their effects on diet quality and physical activity level, (2) evaluate the impact on metabolic risk factors.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • age, high metabolic risk- poor lifestyle habits (diet and physical activity)

Exclusion criteria

  • overt disease

Treatment and study plan

Healthy lifestyle counseling and E-health support

Behavioral

Promotion of healthy lifestyle behaviors through counseling and access to E-health platform

Primary outcomes

  1. Change in blood glucose level

    Time frame: Before ; at 16 weeks; at 12 months

    Blood glucose (mmol/L) assessed using chemistry kits from Ortho-Clinical Diagnostics on a Vitros-5.1 analyzer platform (Clinical Diagnostics, Raritan, NJ, United States)

  2. Change in plasma triglycerides level

    Time frame: Before ; at 16 weeks; at 12 months

    Plasma triglycerides (mmol/L) : assessed using chemistry kits from Ortho-Clinical Diagnostics on a Vitros-5.1 analyzer platform (Clinical Diagnostics, Raritan, NJ, United States)

  3. Change in physical activity level

    Time frame: Before; at 16 weeks; at 12 months

    Minutes in moderate to vigorous physical activity

  4. Change in intakes of healthy food items

    Time frame: Before; at 16 weeks; at 12 months

    number of portions of fruits and vegetables

Secondary outcomes

  1. Change in waist circumference

    Time frame: Before ; at 16 weeks; at 12 months

    waist circumference (cm) assessed by a steel tape

  2. Change in systolic and diastolic blood pressure

    Time frame: Before ; at 16 weeks; at 12 months

    measured manually with a mercury sphygmomanometer

  3. Change in HDL-cholesterol level

    Time frame: Before ; at 16 weeks; at 12 months

    plasma High density lipoprotein- cholesterol: assessed using chemistry kits from Ortho-Clinical

  4. Change in BMI

    Time frame: Before ; at 16 weeks; at 12months

    BMI in kg/m2

Study contacts

Contact information is provided by the study sponsor or research team.

Fawzi Kadi, professor

CONTACT

[email protected]

+4619302160

Sponsors and collaborators

Lead sponsor

Örebro University, Sweden

Other

Registry information

Acronym: PCrorelse

Important dates

Study start
2022
Primary completion
2028
Study completion
2028
First posted
Jan 19, 2023
Registry last updated
Feb 18, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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