Actively Recruiting
Prevention of Lifestyle-related Disorders Based on Functional Examinations
Led by Lena Bornhoft · Updated on 2024-10-08
250
Participants Needed
1
Research Sites
119 weeks
Total Duration
On this page
Sponsors
L
Lena Bornhoft
Lead Sponsor
V
Vastra Gotaland Region
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Prevention of Lifestyle-related Disorders Based on Functional Examinations
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 40 years of age
- Relatively normal general mobility; able to walk without support and use all four extremities without difficulty
- Self-assessed as physically inactive at level 1 or 2 on the Saltin Grimby Physical Activity Level Scale
You will not qualify if you...
- Physical activity verbally reported at level 3 or 4 on Saltin Grimby Physical Activity Level Scale
- Severe mental illness or intellectual impairment
- Pregnancy or receiving hospital-based treatment
- Need for interpreter help without self-arranged assistance
AI-Screening
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Trial Site Locations
Total: 1 location
1
Familjeläkarna i Mölnlycke
Mölnlycke, Region Västra Götaland, Sweden, 43544
Actively Recruiting
Research Team
L
Lena Bornhöft, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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