The Inland Norway Healthy Life Center Study

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorInland Norway University of Applied Sciences

About this trial

Healthy Life Centers (Norwegian, 'Frisklivssentralen') is a municipal service in Norway that aims to promote both physical and mental health, as well as to limit the development of non-communicable diseases. Previous research has shown that receiving follow-up from Healthy Life Centers has led to higher levels of daily physical activity, in addition to improved self-reported health and quality of life among the participants. However, there is a lack of studies that have examined what kind of physiological health effects can be expected from participating in the Healthy Life Center's follow-up.

In this study, responses to the 12-week physical activity program of the Healthy Life Center will be compared with the responses in a negative control group that does not receive such follow-up. Both the intervention group and the reference group (the negative control group) will carry out the same tests and measurements before and after the 12 week period. The tests will include measurements of anthropometric variables (body height, body weight and waist circumference), body composition, arterial stiffness, resting blood pressure and blood variables (blood glucose, long-term blood glucose, blood lipid profile and inflammation markers), in addition to physical tests of mobility, balance, maximum aerobic capacity (maximal oxygen consumption) and maximum muscle strength. Questionnaires related to adherence to the Healthy Life Center follow-up, socio-demographic variables, eating and drinking habits, activity level, perceived physical fitness, motivation for exercise, and health-related quality of life will also be included.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

>18 years of age

Receiving follow-up from the Healthy Life Center

Disqualifiers

In average >1 weekly exercise training session the last three months

>18 years of age

In average >1 weekly exercise training session the last three months

Receiving follow-up from the Healthy Life Center

Trial design

Design model

Parallel

Treatments tested in this trial

  • Physical activity

    Other intervention

    The participants will receive the possibility to attend weekly endurance, resistance and yoga exercise sessions administered by the Healthy Life Center. They will also receive personalized follow-up from the Healthy Life Center, and have the possibility to exercise at the local gym.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Intervention groupActive comparator 1 intervention
Group B: Control groupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Maximal oxygen consumption (measured in mL/kg body mass/min)

Difference in change between the two study arms from before to after the 12-week intervention/control period

Time frame
From before to after the 12-week intervention/control period

Secondary outcomes

1

Balance, measured using the "single leg stance test" (measured in seconds)

Difference in change between the two study arms from before to after the 12-week intervention/control period

Time frame
From before to after the 12-week intervention/control period
2

Mobility, measured using the "sit-and-reach" and the "back stretch" test (measured in centimeters)

Difference in change between the two study arms from before to after the 12-week intervention/control period

Time frame
From before to after the 12-week intervention/control period
3

Fat mass (measured in kilograms)

Difference in change between the two study arms from before to after the 12-week intervention/control period

Time frame
From before to after the 12-week intervention/control period
4

Lean mass (measured in kilograms)

Difference in change between the two study arms from before to after the 12-week intervention/control period

Time frame
From before to after the 12-week intervention/control period

Other outcomes

1

Activity level

Difference in change between the two study arms from before to after the 12-week intervention/control period

Time frame
From before to after the 12-week intervention/control period
2

Adherence to the 12-week intervention (measured as the number of sessions the participant attended divided by the number of sessions prescribed)

For the intervention group

Time frame
During the 12-week intervention
3

Compliance to the 12-week intervention (measured as the number of sessions the participant conducted the session as prescribed divided by the number of total sessions)

For the intervention group

Time frame
During the 12-week intervention

Locations

This trial has no locations.

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: