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Prevention of Lifestyle-related Disorders Based on Functional Examinations

Study acronym: PREVFUNKTION
StatusActive, Not Recruiting
PhaseNot applicable
Started
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Record History

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  1. Minor Enrollment closed, study ongoing
    • Study sites: 1 to 2
    • Primary and study completion dates: Dec 2026 to Jan 2027
    • Start date: Aug 19, 2024 to Aug 28, 2024
    v4
  2. Notable Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 1
    • Start date changed from estimate of Aug 2024 to Aug 19, 2024
    v3
  3. Notable Start date: Apr 2024 to Aug 2024
    • Secondary endpoints: 54 to 56
    v2
  4. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this randomised controlled trial is to examine the effects of functional examinations and feedback/support on healthy 40-year-olds. The main questions it aims to answer are: • Does feedback and motivational interviewing after testing physical function motivate inactive middle-aged people to increase their physical activity level? • Does the intervention lead to health benefits over time - less pain, better function, higher health-related quality of life, fewer risk factors for lifestyle-related illness? Participants will: • undergo medical and functional health examinations, • their physical activity level will be measured, • receive feedback and advice based on both parts of the examinations, • receive a functional profile, • be supported in goalsetting for lifestyle changes. Researchers will compare with a control group who, after the examinations, receive feedback only from the medical examination to see if participants become more physically active, achieve better function, become more motivated to make lifestyle changes, reduce risk factors for lifestyle-related illness, achieve health benefits and better health-related quality of life.
Trial Details
NCT Number NCT06309342
Lead Sponsor Lena Bornhoft
Collaborators: Vastra Gotaland Region, Göteborg University
Conditions
(from sponsor)
Lifestyle-related Condition
Related terms Mental Disorders, Motor Activity
Enrollment 250 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov