Understanding Motivation Towards Exercise to Enhance Physical Activity on

Status Active, not recruiting

Clinical Trial Summary

The goal of this clinical trial is to explore feasibility and evaluate methods to investigate changes in physical activity, function and psychometrics in relation to an exercise intervention in physically inactive middle-aged men and women. The main questions it aims to answer are: - Is the exercise intervention feasible regarding retention and user experience? - Is the evaluation methods on physical activity, function and psychometrics suitable for the present study? - Is there an intervention effect in physical activity, function and psychometrics at three and six month post baseline? - Can barriers and facilitators towards increased physical activity be identified in the two groups of the study? All participants will first receive standard care for physically inactive patients, i.e. Physical activity on Prescription (PaP), followed by allocation to an exercise intervention (EI) group. The EI group will be offered an additional exercise intervention for 12 weeks consisting of 1-2 training sessions per week of a combination of aerobic and resistance training at a private fitness center. Feasibility of the exercise intervention will be evaluated based on retention rates and user experience. Additionally, researchers will assess physical activity, function and psychometrics in the EI group at three and six months to evaluate the suitability of the chosen methods and to get preliminary data on the intervention effect. Finally, interviews with the participants in the control and EI groups will be performed at the end of the study in order to explore barriers and facilitators towards increased physical activity in formally inactive patients. Edit after registration of the study: Due to a lower number of recruited participants than expected (20 instead of the anticipated 30), the protocol was updated by removing the control group that would initially consist of 10 participants. The remaining 20 participants were all allocated to the exercise intervention group to assess feasibility of the intervention.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Physical Inactivity

Clinical Trial Details

NCT number	NCT05691803
Study type	Interventional
Source	Umeå University
Contact
Status	Active, not recruiting
Phase	N/A
Start date	February 3, 2023
Completion date	September 29, 2023

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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Understanding Motivation Towards Exercise to Enhance Physical Activity on Prescription Adherence - Feasibility Study — UMEPA-F

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms