Clinical and Psychosocial Factors Associated With Physical Activity Level in Adults With Marfan Syndrome

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity of Oviedo

About this trial

Background. Marfan syndrome is a genetic connective tissue disorder with cardiovascular and musculoskeletal involvement. Despite clinical advances, many patients exhibit low levels of physical activity, influenced by clinical and psychosocial factors such as fear of exertion, fatigue, or pain. Physical activity behavior in this population remains insufficiently characterized.

Objective. To assess the level of physical activity in adults with Marfan syndrome and to identify the main associated clinical and psychosocial factors, in order to determine predictors of low physical activity.

Methods. An observational, analytical, cross-sectional study will be conducted. Adults with a diagnosis of Marfan syndrome will be included. The primary outcome will be physical activity level, assessed using the International Physical Activity Questionnaire-Short Form. The main independent variables will include kinesiophobia (Tampa Scale for Kinesiophobia), physical activity self-efficacy, perceived fatigue (Fatigue Severity Scale), musculoskeletal pain (Brief Pain Inventory-Short Form), and cardiovascular clinical factors. Potential confounders will include age, sex, body mass index, time since diagnosis, medical recommendations regarding exercise, and current pain. Descriptive analyses and a multivariable logistic regression model will be performed to identify independent predictors of low physical activity.

Expected results. To characterize the level of physical activity in adults with Marfan syndrome and to identify the clinical and psychosocial factors that independently predict low physical activity in this population.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adults (≥18 years).

A confirmed diagnosis of Marfan syndrome according to accepted clinical criteria used in routine follow-up.

Ability to understand and complete an online questionnaire in Spanish.

Access to the internet and an appropriate device to complete the survey.

Disqualifiers

Patients with cognitive impairment or comprehension/literacy difficulties that preclude valid completion of the questionnaires.

Who have experienced a major cardiovascular event or undergone recent cardiovascular/aortic surgery that substantially limits physical activity during the most recent reference period (e.g., within the past 3 months).

With acute conditions or recent musculoskeletal injuries not attributable to Marfan syndrome that markedly restrict physical activity during the previous 7 days (the reference period of the IPAQ-SF).

With incomplete questionnaires for essential variables (IPAQ-SF and/or main predictors)

Trial population

Adults with Marfan syndrome

Trial design

Design model

Cohort

Time perspective

Cross-sectional

Treatments tested in this trial

  • Adults with Marfan syndrome

    Other intervention

    Assessment of psychosocial and clinical factors potentially associated with engagement in physical activity, including kinesiophobia, physical activity self-efficacy, perceived fatigue, musculoskeletal pain, and cardiovascular clinical factors (aortic history and treatment)

Treatment groups

118 Participants
are divided into 1 treatment group
Group A: Observational group1 intervention

Trial outcomes

Primary outcomes

1

Measurement of physical activity level

This variable will be assessed using the validated Spanish version of the International Physical Activity Questionnaire-Short Form (IPAQ-SF). The questionnaire records the frequency (days/week) and duration (minutes/day) of vigorous-intensity activities, moderate-intensity activities, and walking performed during the previous 7 days. Total physical activity will be expressed in MET-minutes per week, calculated according to the official IPAQ scoring protocol (8.0 METs for vigorous activity, 4.0 METs for moderate activity, and 3.3 METs for walking). In addition, physical activity level will be categorized as low, moderate, or high, based on the criteria established by the instrument.

Time frame
Screening visit.

Secondary outcomes

1

Measurement of kinesiophobia (fear of movement or physical exertion)

This variable will be assessed using the Spanish validated version of the Tampa Scale for Kinesiophobia. The scale consists of 11 items with a 4-point Likert-type response format. Total scores range from 11 to 44, with higher scores indicating greater levels of kinesiophobia.

Time frame
Screening visit
2

Measurement of physical activity self-efficacy

This variable will be assessed using the Physical Activity Self-Efficacy Scale, which consists of 10 items evaluating the individual's perceived confidence in maintaining exercise behavior in the presence of common barriers. The total score will be used as a continuous variable, with higher values indicating greater perceived self-efficacy.

Time frame
Screening visit
3

Measurement of perceived fatigue

Perceived fatigue will be assessed using the Fatigue Severity Scale (FSS), which consists of 9 items rated on a scale from 1 (never) to 7 (always). The score will be expressed as the mean of the item responses. A mean score ≥ 4 will be considered indicative of clinically significant fatigue.

Time frame
Screening visit
4

Measurement of musculoskeletal pain

This variable will be assessed using the Spanish version of the Brief Pain Inventory-Short Form (BPI-SF). The pain severity and pain interference subscales will be used, expressed as mean scores on a 0-10 scale, where higher values indicate greater pain intensity or functional interference due to pain.

Time frame
Screening visit

Other outcomes

1

Measurement of age

This variable, considered a potential confounder or moderator, will be measured as a quantitative variable (years).

Time frame
Screening visit
2

Measurement of gender

This variable, considered a potential confounder or moderator, will be measured as a qualitative variable (male/female).

Time frame
Screening visit
3

Measurement of body mass index

This variable, considered a potential confounder or moderator, will be measured as a quantitative variable calculated from body weight (kg) and height (m).

Time frame
Screening visit
4

Measurement of time since diagnosis of Marfan syndrome

This variable, considered a potential confounder or moderator, will be measured as a quantitative variable (years).

Time frame
Screening visit

Sponsors and contacts

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