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Educatieve programma's op basis van gezonde gewoonten om de kwaliteit van leven en psychosociaal profiel bij vrouwen met neurodegeneratieve ziekten te verbeteren: het adviesprotocolonderzoek (fase 2) (ADVICE Phase 2)

29 september 2026 bijgewerkt door: Jacobo Á. Rubio-Arias, Universidad de Almeria

Educatieve programma's op basis van gezonde gewoonten om de kwaliteit van leven en psychosociaal profiel te verbeteren bij vrouwen met neurodegeneratieve ziekten: het adviesprotocolonderzoek

This phase of the project aims to compare in-person, supervised educational programs (EP) with online self-guided EPs in individuals with relapsing-remitting multiple sclerosis. A total of 75 participants will be randomly assigned to one of three groups: a supervised and individualized educational program focused on HIIT training, a supervised and individualized educational program focused on strength training, and a non-supervised, self-guided educational program based on resistance band training. Additionally, sessions on the Mediterranean diet (both supervised and non-supervised) and cognitive-behavioral interventions will be included. A control evaluation will be conducted three months after the intervention to assess the effects of the educational programs, followed by another evaluation three months later to analyze residual effects. Women who participated in Phase 1 of the study will be invited to take part in this second phase.

Studie Overzicht

Studietype

Ingrijpend

Inschrijving (Werkelijk)

40

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

    • Murcia
      • Murcia, Murcia, Spanje, 30120
        • Hospital Universitario Virgen de la Arrixaca

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

18 jaar tot 50 jaar (Volwassen)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

Inclusion criteria include:

  • Women and men of reproductive age (18-45 years) with MS will be included, with the upper age limit adjusted to reflect the reproductive phase;
  • no iron-deficiency anemia;
  • stable disease phase;
  • independent walking ability for over 10 meters.

Women will be recruited first and later matched with men based on age, EDSS, and lifestyle habits (physical activity, smoking, and alcohol consumption).

Exclusion criteria will include participants with MS who:

  • score <1 or >6 on the EDSS;
  • report a relapse within 12 months before the study begins;
  • have taken corticosteroid treatment within the last 2 months;
  • have participated in a structured training program in the previous 6 months.

Once all women with MS are recruited, male participants will be recruited following a 1:1 matching methodology based on age, geographic region, and lifestyle habits.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Ondersteunende zorg
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Verdrievoudigen

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Supervised Strength Training Program (PE1)

Participants will complete 36 strength sessions (3 times a week) at a moderate intensity, 6 educational nutritional intervention sessions, and 8 sessions on energy and fatigue management.

This arm of the study consists of a supervised strength training program, conducted over 12 weeks with three weekly sessions. The sessions follow a wave-like periodization, with intensities ranging from 70% to 85% of 1-RM. Exercises focus on enhancing neuromuscular strength in the lower limbs, such as leg presses and hip extensions, under the supervision of a multidisciplinary team.

Participants will also receive nutritional guidance based on the Mediterranean diet, as well as cognitive-behavioral therapy strategies aimed at optimizing fatigue management and boosting energy levels.

Actieve vergelijker: Self-Guided and Unsupervised Program with General Recommendations (PE1)

Participants will be involved in an unsupervised, self-directed program focusing on physical exercise (three times per week), nutrition and cognitive-behavioral habits.

This arm of the study consists of a self-guided and unsupervised program based on physical exercise (3 times per week), nutrition, and cognitive-behavioral habits. Participants will access online modules that provide guidelines for performing resistance exercises with bands, dietary recommendations following the principles of the Mediterranean diet, and cognitive-behavioral techniques for fatigue management.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Satisfaction with Physical Activity
Tijdsspanne: Baseline (pre-intervention)

Satisfaction with Physical Activity will be measured using an eight-item, 5-point Likert scale

Baseline (pre-intervention)
Satisfaction with Physical Activity
Tijdsspanne: Immediately after the intervention

Satisfaction with Physical Activity will be measured using an eight-item, 5-point Likert scale

Immediately after the intervention
Visual Analogue Scale for Fatigue (VAS-F)
Tijdsspanne: Immediately before each of the 36 exercise sessions (pre-session assessment).

The Visual Analogue Scale for Fatigue (VAS-F) assesses subjective levels of fatigue and energy

Immediately before each of the 36 exercise sessions (pre-session assessment).
Visual Analogue Scale for Fatigue (VAS-F)
Tijdsspanne: Immediately after each of the 36 exercise sessions (post-session assessment).

The Visual Analogue Scale for Fatigue (VAS-F) assesses subjective levels of fatigue and energy

Immediately after each of the 36 exercise sessions (post-session assessment).
Modified Fatigue Impact Scale (MFIS)
Tijdsspanne: Baseline (pre-intervention).

Fatigue perception will be measured using the MFIS. This scale is a 21-item multidimensional questionnaire that evaluates the physical, cognitive, and psychosocial effects of fatigue on a five-point ordinal scale (with a maximum total score of 84).

Baseline (pre-intervention).
Modified Fatigue Impact Scale (MFIS)
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

Fatigue perception will be measured using the MFIS. This scale is a 21-item multidimensional questionnaire that evaluates the physical, cognitive, and psychosocial effects of fatigue on a five-point ordinal scale (with a maximum total score of 84)

48 hours after the last exercise session (post-intervention assessment).

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Inflammatory Profile
Tijdsspanne: Baseline (pre-intervention).

The inflammatory profile evaluates key cytokines, including IFN-γ, IL-6, TNF-α, IL-10, and TGF-β1, to assess systemic inflammation and immune response dynamics

Baseline (pre-intervention).
Inflammatory Profile
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

The inflammatory profile evaluates key cytokines, including IFN-γ, IL-6, TNF-α, IL-10, and TGF-β1, to assess systemic inflammation and immune response dynamics

48 hours after the last exercise session (post-intervention assessment).
The hormonal profile
Tijdsspanne: Pre-intervention in each phase of the menstrual cycle (early follicular phase, late follicular phase and mid-luteal phase).

The hormonal profile includes the assessment of TSH, progesterone (PG), luteinizing hormone (LH), follicle-stimulating hormone (FSH), estradiol, and testosterone to evaluate endocrine function, menstrual cycle phases, and hormonal balance.

Pre-intervention in each phase of the menstrual cycle (early follicular phase, late follicular phase and mid-luteal phase).
Cognitive Function
Tijdsspanne: Baseline (pre-intervention).

Brain-Derived Neurotrophic Factor (BDNF) is a protein involved in neuroplasticity, cognitive function, and neuronal survival, serving as a blood biomarker for brain health and adaptability.

Baseline (pre-intervention).
Cognitive Function
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

Brain-Derived Neurotrophic Factor (BDNF) is a protein involved in neuroplasticity, cognitive function, and neuronal survival, serving as a blood biomarker for brain health and adaptability

48 hours after the last exercise session (post-intervention assessment).
Neurofilament Light Chain (NFL)
Tijdsspanne: Baseline (pre-intervention).

Neurofilament light chain (NFL) is one of the most relevant biomarkers in multiple sclerosis (MS). The Simoa detection technique (ultrasensitive single-molecule array) allows its analysis in serum, providing both the total value and the Z-Score, enabling precise assessment of axonal damage and disease progression.

Baseline (pre-intervention).
Neurofilament Light Chain (NFL)
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

Neurofilament light chain (NFL) is one of the most relevant biomarkers in multiple sclerosis (MS). The Simoa detection technique (ultrasensitive single-molecule array) allows its analysis in serum, providing both the total value and the Z-Score, enabling precise assessment of axonal damage and disease progression.

48 hours after the last exercise session (post-intervention assessment).
Physical Self-Perception
Tijdsspanne: Baseline (pre-intervention).

Physical self-perception will be evaluated using six subscales-sports competence, physical condition, body attractiveness, physical strength, general physical self-perception, and overall self-perception-on a 5-point Likert scale

Baseline (pre-intervention).
Physical Self-Perception
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

Physical self-perception will be evaluated using six subscales-sports competence, physical condition, body attractiveness, physical strength, general physical self-perception, and overall self-perception-on a 5-point Likert scale

48 hours after the last exercise session (post-intervention assessment).
Walking Endurance
Tijdsspanne: Baseline (pre-intervention).

Participants will undergo the 2-minute walk test, during which they will walk at their preferred, self-selected speed to assess walking endurance. The test course will be rectangular, with corners marked by cones. Participants will be allowed to rest during the test, if necessary, but the clock will not stop during these rest periods. The total distance covered will be recorded

Baseline (pre-intervention).
Walking Endurance
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

Participants will undergo the 2-minute walk test, during which they will walk at their preferred, self-selected speed to assess walking endurance. The test course will be rectangular, with corners marked by cones. Participants will be allowed to rest during the test, if necessary, but the clock will not stop during these rest periods. The total distance covered will be recorded

48 hours after the last exercise session (post-intervention assessment).
Pain Catastrophizing
Tijdsspanne: Baseline (pre-intervention).

The Pain Catastrophizing Scale will measure catastrophic thoughts related to pain, focusing on rumination and helplessness, with responses on a similar scale

Baseline (pre-intervention).
Pain Catastrophizing
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

The Pain Catastrophizing Scale will measure catastrophic thoughts related to pain, focusing on rumination and helplessness, with responses on a similar scale

48 hours after the last exercise session (post-intervention assessment).
Quality of Life questionnaire
Tijdsspanne: Baseline (pre-intervention).

The Multiple Sclerosis Quality of Life-54 will gauge quality of life across 14 subscales, yielding physical and mental health composite scores

Baseline (pre-intervention).
Quality of Life questionnaire
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

The Multiple Sclerosis Quality of Life-54 will gauge quality of life across 14 subscales, yielding physical and mental health composite scores

48 hours after the last exercise session (post-intervention assessment).
State-Trait Anxiety
Tijdsspanne: Baseline (pre-intervention).

Description: The State-Trait Anxiety Inventory will measure both situational and general anxiety on a 4-point scale

Baseline (pre-intervention).
State-Trait Anxiety
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

The State-Trait Anxiety Inventory will measure both situational and general anxiety on a 4-point scaleTime Frame: Before the first training session

48 hours after the last exercise session (post-intervention assessment).
Rate of force development
Tijdsspanne: Baseline (pre-intervention).

Participants will sit in a chair with both legs flexed at a 90-degree angle, and the tested ankle securely attached to a customized device with a load cell (MuscleLab Force Sensor, Ergotest AS, Langesund, Norway). They will perform three maximum contractions, each lasting 2 seconds, with 3 minutes of rest in between. The RFD will be analyzed. Testing will begin with the right leg, and the repetition with the highest recorded value for each leg will be used in the analysis

Baseline (pre-intervention).
Rate of force development
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

Participants will sit in a chair with both legs flexed at a 90-degree angle, and the tested ankle securely attached to a customized device with a load cell (MuscleLab Force Sensor, Ergotest AS, Langesund, Norway). They will perform three maximum contractions, each lasting 2 seconds, with 3 minutes of rest in between. The RFD will be analyzed. Testing will begin with the right leg, and the repetition with the highest recorded value for each leg will be used in the analysis

48 hours after the last exercise session (post-intervention assessment).
Maximum Voluntary Isometric Contraction
Tijdsspanne: Baseline (pre-intervention).

Participants will sit in a chair with both legs flexed at a 90-degree angle, and the tested ankle securely attached to a customized device with a load cell (MuscleLab Force Sensor, Ergotest AS, Langesund, Norway).Participants will perform three 5-second MVIC, with 3 minutes of rest in between. Testing will always begin with the right leg, and the contraction with the highest recorded MVIC value will be used in the analysis Time Frame: Before the first training session

Baseline (pre-intervention).
Maximum Voluntary Isometric Contraction
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

Participants will sit in a chair with both legs flexed at a 90-degree angle, and the tested ankle securely attached to a customized device with a load cell (MuscleLab Force Sensor, Ergotest AS, Langesund, Norway).Participants will perform three 5-second MVIC, with 3 minutes of rest in between. Testing will always begin with the right leg, and the contraction with the highest recorded MVIC value will be used in the analysis Time Frame: Before the first training session

48 hours after the last exercise session (post-intervention assessment).
Maximal neural drive
Tijdsspanne: Baseline (pre-intervention).

To measure neural drive, the electromyographic activity (sEMG) of the right leg's vastus lateralis will be recorded during the MVIC (Delsys Trigno, Delsys Inc., Boston, MA) with skin prepared and electrode positioning following SENIAM guidelines. EMG peak will be analyzed. The EMG peak during MVIC will represent the maximum neural drive

Baseline (pre-intervention).
Maximal neural drive
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

To measure neural drive, the electromyographic activity (sEMG) of the right leg's vastus lateralis will be recorded during the MVIC (Delsys Trigno, Delsys Inc., Boston, MA) with skin prepared and electrode positioning following SENIAM guidelines. EMG peak will be analyzed. The EMG peak during MVIC will represent the maximum neural drive

48 hours after the last exercise session (post-intervention assessment).
Central activation ratio
Tijdsspanne: Baseline (pre-intervention).

Two bipolar electrodes (10×15 cm) will be placed on the right quadriceps, with electrical stimulation controlled by Signal 6.0 software (CED, Cambridge, England) at 100 Hz frequency, 50 pulses, 0.009 s pulse duration, and 0.01 s interval, set to 40-50% of MVIC. Central activation ratio (CAR) will be assessed through a sequence of one supramaximal twitch, a 100 Hz tetanic train, an MVIC with superimposed tetanic train, followed by a potentiated tetanic train and a potentiated supramaximal twitch. This sequence will be repeated twice with 2-minute rests, and twitch-to-tetanus ratio, MVIC peak, and maximum force values will be calculated for CAR. The CAR will be calculated using the following formula: "CAR= " "Force during MVIC" /"Force during MVIC + supramaximal stimulation"

Baseline (pre-intervention).
Central activation ratio
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

Two bipolar electrodes (10×15 cm) will be placed on the right quadriceps, with electrical stimulation controlled by Signal 6.0 software (CED, Cambridge, England) at 100 Hz frequency, 50 pulses, 0.009 s pulse duration, and 0.01 s interval, set to 40-50% of MVIC. Central activation ratio (CAR) will be assessed through a sequence of one supramaximal twitch, a 100 Hz tetanic train, an MVIC with superimposed tetanic train, followed by a potentiated tetanic train and a potentiated supramaximal twitch. This sequence will be repeated twice with 2-minute rests, and twitch-to-tetanus ratio, MVIC peak, and maximum force values will be calculated for CAR. The CAR will be calculated using the following formula: "CAR= " "Force during MVIC" /"Force during MVIC + supramaximal stimulation"

48 hours after the last exercise session (post-intervention assessment).
Upper Limb Maximum Strength
Tijdsspanne: Baseline (pre-intervention).

Isometric grip strength will be measured with an electronic dynamometer (K-Force Grip, Kinvent, Montpellier, France) as participants stand with elbows extended. Each hand will perform 3 trials, with 30 seconds rest between attempts

Baseline (pre-intervention).
Upper Limb Maximum Strength
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

Isometric grip strength will be measured with an electronic dynamometer (K-Force Grip, Kinvent, Montpellier, France) as participants stand with elbows extended. Each hand will perform 3 trials, with 30 seconds rest between attempts

48 hours after the last exercise session (post-intervention assessment).
Spasticity
Tijdsspanne: Before the first session of the intervention program

The Pendulum Test is used to assess the level of spasticity by evaluating the resistance to passive movement in the affected limb. The test involves moving the limb in a pendulum-like motion and observing the fluidity of the movement, with increased resistance indicating higher spasticity levels

Before the first session of the intervention program
Spasticity
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

The Pendulum Test is used to assess the level of spasticity by evaluating the resistance to passive movement in the affected limb. The test involves moving the limb in a pendulum-like motion and observing the fluidity of the movement, with increased resistance indicating higher spasticity levels

48 hours after the last exercise session (post-intervention assessment).
Intrinsic muscle characteristics
Tijdsspanne: Baseline (pre-intervention).

Muscle characteristics (frequency, stiffness, degradation) assessed with MyotonPRO (MyotonPRO, Myoton AS, Estonia)

Baseline (pre-intervention).
Intrinsic muscle characteristics
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

Muscle characteristics (frequency, stiffness, degradation) assessed with MyotonPRO (MyotonPRO, Myoton AS, Estonia)

48 hours after the last exercise session (post-intervention assessment).
Gait speed
Tijdsspanne: Baseline (pre-intervention).

Gait speed will be determined with the 10-meter walk test using two photocells (Ergotest Technology AS, Langesund, Norway) at 5 and 10 meters; participants will complete two maximum-speed trials, with the slower time recorded

Baseline (pre-intervention).
Gait speed
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

Gait speed will be determined with the 10-meter walk test using two photocells (Ergotest Technology AS, Langesund, Norway) at 5 and 10 meters; participants will complete two maximum-speed trials, with the slower time recorded

48 hours after the last exercise session (post-intervention assessment).
Static balance with eyes open
Tijdsspanne: Baseline (pre-intervention).

Balance is measured with static trials on a force platform (Ergotest Technology AS, Langesund, Norway), where participants stand barefoot with arms at their sides for two 30-second trials each

Baseline (pre-intervention).
Static balance with eyes open
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

Balance is measured with static trials on a force platform (Ergotest Technology AS, Langesund, Norway), where participants stand barefoot with arms at their sides for two 30-second trials each

48 hours after the last exercise session (post-intervention assessment).
Static balance with eyes closed
Tijdsspanne: Baseline (pre-intervention).

Balance is measured with static trials on a force platform (Ergotest Technology AS, Langesund, Norway), where participants stand barefoot with arms at their sides for two 30-second trials each

Baseline (pre-intervention).
Static balance with eyes closed
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

Balance is measured with static trials on a force platform (Ergotest Technology AS, Langesund, Norway), where participants stand barefoot with arms at their sides for two 30-second trials each

48 hours after the last exercise session (post-intervention assessment).
Sit-to-stand
Tijdsspanne: Baseline (pre-intervention).

The sit-to-stand test requires participants to rise as quickly as possible from a seated position with 90º knee flexion and arms crossed

Baseline (pre-intervention).
Sit-to-stand
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

The sit-to-stand test requires participants to rise as quickly as possible from a seated position with 90º knee flexion and arms crossed

48 hours after the last exercise session (post-intervention assessment).
Timed Up-and-Go test
Tijdsspanne: Baseline (pre-intervention).

In the Timed Up-and-Go test, participants move from sitting to standing, walk 3 meters, turn, return, and sit

Baseline (pre-intervention).
Timed Up-and-Go test
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

In the Timed Up-and-Go test, participants move from sitting to standing, walk 3 meters, turn, return, and sit

48 hours after the last exercise session (post-intervention assessment).
Delayed onset muscle soreness
Tijdsspanne: Baseline (pre-intervention).

To measure delayed onset muscle soreness (DOMS), a 10-point visual analogue scale shall be used, where 1 = no pain and 10 = intolerable pain

Baseline (pre-intervention).
Subjective Perception of Effort
Tijdsspanne: Baseline (pre-intervention).

Participants will be instructed and familiarized with the use of the RPE scale during the familiarization phase. RPE will be assessed before, during (after each exercise within the session), and after the training session using the Borg 6-20 RPE scale

Baseline (pre-intervention).
Fatigue Visual Analog Scale (VAS-F)
Tijdsspanne: Baseline (pre-intervention).

The VAS-F will be used to measure fatigue. This scale, is subdivided into two subscales: fatigue and energy. The VAS-F features a 100 mm long horizontal line, with the term "none" at one end and "very severe" at the opposite end. Participants are required to mark the point on the line corresponding to their perception of the severity of fatigue between these two endpoints.

Baseline (pre-intervention).
Anthropometric
Tijdsspanne: Baseline (pre-intervention).

Anthropometric measurements will be taken to assess body morphology, fat distribution, and potential alterations due to multiple sclerosis (MS), such as muscle atrophy or changes in body fat percentage. These measurements provide valuable information regarding comorbidities, including abdominal obesity and cardiovascular risk, which are particularly relevant in MS due to factors like reduced mobility or medication use

Baseline (pre-intervention).
Anthropometric
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

Anthropometric measurements will be taken to assess body morphology, fat distribution, and potential alterations due to multiple sclerosis (MS), such as muscle atrophy or changes in body fat percentage. These measurements provide valuable information regarding comorbidities, including abdominal obesity and cardiovascular risk, which are particularly relevant in MS due to factors like reduced mobility or medication use

48 hours after the last exercise session (post-intervention assessment).
Bioimpedance
Tijdsspanne: Baseline (pre-intervention).

Bioimpedance will be used to assess body composition, including body fat percentage, lean mass, and total body water. These measurements are important for understanding changes in body composition due to multiple sclerosis (MS), as the disease can impact muscle mass, fluid balance, and fat distribution. Bioimpedance provides valuable insight into the health status and nutritional needs of individuals with MS

Baseline (pre-intervention).
Bioimpedance
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

Bioimpedance will be used to assess body composition, including body fat percentage, lean mass, and total body water. These measurements are important for understanding changes in body composition due to multiple sclerosis (MS), as the disease can impact muscle mass, fluid balance, and fat distribution. Bioimpedance provides valuable insight into the health status and nutritional needs of individuals with MS

48 hours after the last exercise session (post-intervention assessment).
Physical Activity Levels
Tijdsspanne: Baseline (pre-intervention).

To assess physical activity in patients with multiple sclerosis (MS), both the International Physical Activity Questionnaire (IPAQ) and triaxial accelerometers can be adapted to account for the mobility limitations often experienced by these individuals. The IPAQ can be tailored by including questions that specifically address low-impact or moderate-intensity activities, considering factors such as fatigue and muscle weakness. Triaxial accelerometers, which measure movement in three planes (vertical, lateral, and anterior-posterior), provide a more detailed and precise measurement of physical activity, capturing even small movements or low-intensity activities such as walking short distances. Together, these tools allow for a comprehensive assessment of physical activity levels in MS patients, while considering their unique needs and capabilities. Additionally, the MET (Metabolic Equivalent of Task) methodology should be adjusted to reflect the lower intensity of activities commonly p

Baseline (pre-intervention).
Physical Activity Levels
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

To assess physical activity in patients with multiple sclerosis (MS), both the International Physical Activity Questionnaire (IPAQ) and triaxial accelerometers can be adapted to account for the mobility limitations often experienced by these individuals. The IPAQ can be tailored by including questions that specifically address low-impact or moderate-intensity activities, considering factors such as fatigue and muscle weakness. Triaxial accelerometers, which measure movement in three planes (vertical, lateral, and anterior-posterior), provide a more detailed and precise measurement of physical activity, capturing even small movements or low-intensity activities such as walking short distances. Together, these tools allow for a comprehensive assessment of physical activity levels in MS patients, while considering their unique needs and capabilities. Additionally, the MET (Metabolic Equivalent of Task) methodology should be adjusted to reflect the lower intensity of activities commonly p

48 hours after the last exercise session (post-intervention assessment).
Dietary and Nutritional Follow-up
Tijdsspanne: Baseline (pre-intervention).

Mediterranean Diet adherence questionnaires and food diaries could be effective tools for evaluating nutrition, particularly if MS patients have poor consumption of essential nutrients for their overall health

Baseline (pre-intervention).
Dietary and Nutritional Follow-up
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

Mediterranean Diet adherence questionnaires and food diaries could be effective tools for evaluating nutrition, particularly if MS patients have poor consumption of essential nutrients for their overall health

48 hours after the last exercise session (post-intervention assessment).
The Kurtzke Disability Scale
Tijdsspanne: Baseline (pre-intervention).

The Kurtzke Disability Scale (EDSS) is divided into 8 functional systems (FS); four primary: pyramidal function, cerebellar function, sensory function, and brainstem function; and four secondary: sphincters, vision, mental, and others. For each FS, a severity score is provided, ranging from 0 to 6 or 7. The overall score of the scale is measured on a 20-item scale (from 0 to 10 points, increasing in half-point increments). Up to 3.5, the score obtained in each FS and the number of affected FS automatically determine the EDSS score. From 4 to 7, the definition of each level is also given by the ability to walk (ability to walk without stopping, need for assistance)

Baseline (pre-intervention).
The Kurtzke Disability Scale
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

The Kurtzke Disability Scale (EDSS) is divided into 8 functional systems (FS); four primary: pyramidal function, cerebellar function, sensory function, and brainstem function; and four secondary: sphincters, vision, mental, and others. For each FS, a severity score is provided, ranging from 0 to 6 or 7. The overall score of the scale is measured on a 20-item scale (from 0 to 10 points, increasing in half-point increments). Up to 3.5, the score obtained in each FS and the number of affected FS automatically determine the EDSS score. From 4 to 7, the definition of each level is also given by the ability to walk (ability to walk without stopping, need for assistance).

48 hours after the last exercise session (post-intervention assessment).
Subjective Sleep Quality Questionnaire
Tijdsspanne: Baseline (pre-intervention).

Subjective sleep quality will be measured using the Karolinska Sleep Diary questionnaire [73]. The questionnaire includes the following items: a) sleep quality (very poor [1] - very good [5]), b) sleep tranquility (very restless [1] - very calm [5]), c) ease of falling asleep (very difficult [1] - very easy [5]), d) awakenings (woke up too early [1] - did not wake up early [3]), e) ease of waking up (very difficult [1] - very easy [5]), f) feeling of rest (did not rest at all [1] - fully rested [3]), and g) sufficient sleep (no, definitely too little [1] - yes, definitely enough [5]).

Baseline (pre-intervention).
Subjective Sleep Quality Questionnaire
Tijdsspanne: 48 hours after the last exercise session (post-intervention assessment).

Subjective sleep quality will be measured using the Karolinska Sleep Diary questionnaire [73]. The questionnaire includes the following items: a) sleep quality (very poor [1] - very good [5]), b) sleep tranquility (very restless [1] - very calm [5]), c) ease of falling asleep (very difficult [1] - very easy [5]), d) awakenings (woke up too early [1] - did not wake up early [3]), e) ease of waking up (very difficult [1] - very easy [5]), f) feeling of rest (did not rest at all [1] - fully rested [3]), and g) sufficient sleep (no, definitely too little [1] - yes, definitely enough [5]).

48 hours after the last exercise session (post-intervention assessment).
Sleep Quality Measured by Actigraph
Tijdsspanne: The week prior to the start of the intervention. Baseline (pre-intervention).

Sleep quality based on actigraphy will be evaluated using the Actiwatch wGT3X-BT activity monitoring system (Cambridge Neurotechnology, Cambridge, UK) [74]. This device uses a piezoelectric accelerometer to measure activity. Participants will wear the Actiwatch on their non-dominant wrist. The lower sensitivity threshold for actigraphy will be set at 80 counts/epoch. Data analysis will begin at the start of the nighttime rest period (bedtime) and conclude at the start of daytime activity (wake-up time).

The week prior to the start of the intervention. Baseline (pre-intervention).
Sleep Quality Measured by Actigraph
Tijdsspanne: The week following the completion of the intervention (post-intervention assessment).

Sleep quality based on actigraphy will be evaluated using the Actiwatch wGT3X-BT activity monitoring system (Cambridge Neurotechnology, Cambridge, UK) [74]. This device uses a piezoelectric accelerometer to measure activity. Participants will wear the Actiwatch on their non-dominant wrist. The lower sensitivity threshold for actigraphy will be set at 80 counts/epoch. Data analysis will begin at the start of the nighttime rest period (bedtime) and conclude at the start of daytime activity (wake-up time)

The week following the completion of the intervention (post-intervention assessment).
Delayed onset muscle soreness
Tijdsspanne: Immediately after each physical exercise session (post-intervention assessment).

To measure delayed onset muscle soreness (DOMS), a 10-point visual analogue scale shall be used, where 1 = no pain and 10 = intolerable pain

Immediately after each physical exercise session (post-intervention assessment).
Subjective Perception of Effort
Tijdsspanne: Immediately after each physical exercise session (post-intervention assessment).

Participants will be instructed and familiarized with the use of the RPE scale during the familiarization phase. RPE will be assessed before, during (after each exercise within the session), and after the training session using the Borg 6-20 RPE scale

Immediately after each physical exercise session (post-intervention assessment).
Fatigue Visual Analog Scale (VAS-F)
Tijdsspanne: Immediately after each physical exercise session (post-intervention assessment).

The VAS-F will be used to measure fatigue. This scale, is subdivided into two subscales: fatigue and energy. The VAS-F features a 100 mm long horizontal line, with the term "none" at one end and "very severe" at the opposite end. Participants are required to mark the point on the line corresponding to their perception of the severity of fatigue between these two endpoints.

Immediately after each physical exercise session (post-intervention assessment).

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

15 april 2025

Primaire voltooiing (Werkelijk)

15 juni 2025

Studie voltooiing (Werkelijk)

28 juli 2026

Studieregistratiedata

Eerst ingediend

20 februari 2025

Eerst ingediend dat voldeed aan de QC-criteria

13 maart 2025

Eerst geplaatst (Werkelijk)

19 maart 2025

Updates van studierecords

Laatste update geplaatst (Werkelijk)

30 september 2026

Laatste update ingediend die voldeed aan QC-criteria

29 september 2026

Laatst geverifieerd

1 september 2026

Meer informatie

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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