MedPath

Prevention of Lifestyle-related Ill-health With Early Functional Examinations and Individualized Risk Profiles

Not Applicable
Completed
Conditions
Lifestyle Risk Reduction
Interventions
Behavioral: Risk profile
Registration Number
NCT05535296
Lead Sponsor
Lena Bornhoft
Brief Summary

Background: Many lifestyle-related health disorders are influenced by physical activity level and physical function. Health examinations which focus on musculoskeletal function of people who have risk factors for lifestyle-related disorders, combined with person-centered advice based on risk profiles can give people knowledge and guidance to manage their own lifestyle priorities.

Aim: To investigate the feasibility of a protocol for a randomized controlled trial (RCT) which will examine the preventive effects of musculoskeletal function examinations and person-centered advice on inactive middle-aged people.

Methods: Physically inactive middle-aged people will be invited to participate in a two-part health examination with follow-up after three months in a pilot study. Part 1 is a standard health examination including blood tests and Part 2 is a functional examination of fitness, strength, mobility, balance and posture according to our protocol based on validated tests. The intervention group receives feedback based on both parts of the examination while the control group receives feedback only from Part 1. Physical activity level will be measured objectively with accelerometers at inclusion and follow-up.

Expected results: The pilot study is expected to show whether the planned RCT is practically feasible and to give relevant support for the power analysis for a later full-scale RCT. Better understanding of personal physical function and risk factors can facilitate lifestyle decisions on the individual level which can reduce the risk for later ill-health and need of health-care. Preventive interventions may contribute to reduce the ever-increasing level of lifestyle-related ill-health.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
27
Inclusion Criteria
  • Born 1982 (aged 40 years). Self-assessed as physically inactive. Self-reported normal general mobility - can walk without support and has full use of all 4 extremities.
Exclusion Criteria
  • Self-reported regular moderate-to-intensive physical activity more than once per week. Pregnancy. Ongoing treatment requiring hospital-based services. Severe mental illness or intellectual impairment. Need of interpreter to participate in the study or answer the questionnaires.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intervention groupRisk profileStandard health examination and related feedback. Functional examination. Risk profile and related advice.
Primary Outcome Measures
NameTimeMethod
Physical activity levelChange between inclusion and 3-4 month follow-up.

Mean number of daily minutes in moderate-to-intensive physical activity measured with accelerometers during one week.

Participant feedbackMeasured at 3-4 month follow-up.

Rating of overall helpfulness of intervention in intervention group on 0 to 5 numerical rating scale ranging between 0=No help at all and 5=Very helpful.

Secondary Outcome Measures
NameTimeMethod
Occiput-to-wall testChange between inclusion and 3-4 month follow-up.

Measured as contact or no contact between head and wall.

Patella mobilityChange between inclusion and 3-4 month follow-up.

Measured as locked or not locked patella in habitual standing position.

Number of pain locationsChange between inclusion and 3-4 month follow-up.

Change in number of pain locations on pain diagram.

Waist circumferenceChange between inclusion and 3-4 month follow-up.

Measured in centimeters with measuring tape.

Navicular Drop testChange between inclusion and 3-4 month follow-up.

Measured as drop distance in millimeters, with higher numbers indicating higher dgree of pronation.

Participant feedback functional tests-Borg follow-upMeasured at 3-4 month follow-up.

Rating of difficulty of individual functional tests on the Borg Rating of Perceived Exertion scale, ranging from 6 to 20 with higher levels indicating higher exertion level.

Participant feedback - descriptive follow-upRecorded at 3-4 month follow-up.

Voluntary subjective impressions of the intervention

Plank testChange between inclusion and 3-4 month follow-up.

Measured with maximum endurance time, with longer time indicating better trunk strength.

Sharpened RombergChange between inclusion and 3-4 month follow-up.

Measured with maximum endurance time, with higher numbers indicating better balance.

Lateral Reach testChange between inclusion and 3-4 month follow-up.

Measured with reach limit in centimeters, with higher numbers indicating better balance.

Sit-rise testChange between inclusion and 3-4 month follow-up.

Measured as points on 0-10 scale, with higher numbers indicating better mobility.

Participant feedback functional tests-Borg inclusionMeasured at inclusion.

Rating of difficulty of individual functional tests on the Borg Rating of Perceived Exertion scale, ranging from 6 to 20 with higher levels indicating higher exertion level.

Participant feedback - descriptive inclusionRecorded at inclusion.

Voluntary subjective impressions of the intervention

2-minute step testChange between inclusion and 3-4 month follow-up.

Measured with number of steps, where higher values indicate better fitness level.

Participant feedback functional tests-instructionsMeasured at inclusion.

Rating of how understandable the instructions were on a 0 to 5 numerical rating scale where 0 is completely ununderstandable and 5 is very easy to understand.

Risk levelsChange between inclusion and 3-4 month follow-up.

Change in risk levels on the risk profile.

Ekblom-Bak fitness testChange between inclusion and 3-4 month follow-up.

Measured as VO2-max in ml/kg/min where higher values indicate better fitness level.

Sorenson's back extension testChange between inclusion and 3-4 month follow-up.

Measured with maximum endurance time, with longer time indicating better trunk strength.

Goal achievement3-4 month follow-up

Proportion of goals set at inclusion achieved.

Handgrip strengthChange between inclusion and 3-4 month follow-up.

Measured with Jamar dynamometer, with higher numbers indicating greater strength.

Body mass indexChange between inclusion and 3-4 month follow-up.

Calculated by weight in kg divided by squared height in meters.

30-second biceps testChange between inclusion and 3-4 month follow-up.

Measured by maximum number of repetitions with 2 kg (women) or 4 kg (men) dumbbell during 30 seconds, with higher numbers indicating greater strength.

Stand-on-one-leg eyes-closed testChange between inclusion and 3-4 month follow-up.

Measured with maximum endurance time, with higher numbers indicating better balance.

Functional Reach testChange between inclusion and 3-4 month follow-up.

Measured with reach limit in centimeters, with higher numbers indicating better balance.

Unilateral heel rise testChange between inclusion and 3-4 month follow-up.

Measured with maximum number of repetitions per leg, with higher numbers indicating greater strength.

30-second chair stand testChange between inclusion and 3-4 month follow-up.

Measured with maximum number of repetitions during 30 seconds, with higher numbers indicating greater strength.

Stand-on-one-leg eyes-open testChange between inclusion and 3-4 month follow-up.

Measured with maximum endurance time, with higher numbers indicating better balance.

Fingertip-floor testChange between inclusion and 3-4 month follow-up.

Measured as distance in centimeters, with higher numbers indicating lower mobility.

Beighton's hypermobility scoreMeasured at inclusion.

Measured on 0 to 9 scale with higher numbers indicating higher level of hypermobility

Risk for developing long-term musculoskeletal disordersChange between inclusion and 3-4 month follow-up.

Measured with the Örebro Musculoskeletal Pain Screening Questionnaire (10 questions, max 100 points, higher values indicate increased risk for longterm pain.

Blood pressureChange between inclusion and 3-4 month follow-up.

Change in blood pressure.

Blood testsChange between inclusion and 3-4 month follow-up.

Whether or not acceptable levels of serum cholesterol (3.3 to 6.9mmol/L), triglycerides (0.45 to 2.6 mmol/L), LDL-cholesterol (1.4 to 4.7 mmol/L), HDL cholesterol (women 1.0 to 2.7 and men 0.80 to 2.1 mmol/L) and blood glucose (4.0 to 6.0 mmol/L).

Supine bridge testChange between inclusion and 3-4 month follow-up.

Measured with maximum endurance time, with longer time indicating better trunk strength.

Lateral flexion testChange between inclusion and 3-4 month follow-up.

Measured as distance in millimeters, with higher numbers indicating better mobility.

Health-related quality of lifeChange between inclusion and 3-4 month follow-up.

Measured with Euroqol-5 dimensions, 5 questions and 0-100 barometer. Higher scores indicate better quality of life.

Self-reported physical activity_SGPALSChange between inclusion and 3-4 month follow-up.

Measured with Saltin-Grimby Physical Activity Level Scale (0 to 4 descriptive levels). Higher levels indicate more physically active.

Sedentary timeChange between inclusion and 3-4 month follow-up.

Measured with the SED-GIH question on time sitting still (7 levels from almost always to never). Higher levels indicate more physically active.

Self-reported physical activity_SNBHWChange between inclusion and 3-4 month follow-up.

Measured with the Swedish National Board of Health and Welfare's 2 questions on physical activity (choose from 6 descriptive levels of exercise and 7 descriptive levels of daily activity). Higher levels indicate more physically active.

Trial Locations

Locations (1)

Närhälsan Biskopsgården Health centre

🇸🇪

Gothenburg, Sweden

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