Educational Programs Based on Healthy Habits to Improve Quality of Life and Psychosocial Profile in Women With Neurodegenerative Diseases: The ADVICE Protocol Study (Phase 1)

Satisfaction with Physical Activity will be measured using an 8-item scale. Items are rated on a 5-point Likert scale ranging from 1 (Totally disagree) to 5 (Totally agree). Total scores range from 8 to 40, with higher scores indicating greater satisfaction with physical activity.

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).

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).

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).

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).

The Visual Analogue Scale for Fatigue (VAS-F) assesses subjective perceptions of fatigue on a scale from 0 to 10, where 0 indicates no fatigue at all and 10 indicates extreme fatigue. Higher scores reflect greater perceived fatigue.

The Visual Analogue Scale for Fatigue (VAS-F) assesses subjective perceptions of fatigue on a scale from 0 to 10, where 0 indicates no fatigue at all and 10 indicates extreme fatigue. Higher scores reflect greater perceived fatigue.

The Visual Analogue Scale for Fatigue (VAS-F) assesses subjective perceptions of fatigue on a scale from 0 to 10, where 0 indicates no fatigue at all and 10 indicates extreme fatigue. Higher scores reflect greater perceived fatigue.

The Visual Analogue Scale for Fatigue (VAS-F) assesses subjective perceptions of fatigue on a scale from 0 to 10, where 0 indicates no fatigue at all and 10 indicates extreme fatigue. Higher scores reflect greater perceived fatigue.

The Visual Analogue Scale for Energy (VAS-E) assesses subjective perceptions of Energy on a scale from 0 to 10, where 0 indicates no energy at all and 10 indicates maximum energy. Higher scores reflect greater perceived energy.

The Visual Analogue Scale for Energy (VAS-E) assesses subjective perceptions of Energy on a scale from 0 to 10, where 0 indicates no energy at all and 10 indicates maximum energy. Higher scores reflect greater perceived energy.

The Visual Analogue Scale for Energy (VAS-E) assesses subjective perceptions of Energy on a scale from 0 to 10, where 0 indicates no energy at all and 10 indicates maximum energy. Higher scores reflect greater perceived energy.

The Visual Analogue Scale for Energy (VAS-E) assesses subjective perceptions of Energy on a scale from 0 to 10, where 0 indicates no energy at all and 10 indicates maximum energy. Higher scores reflect greater perceived energy.

The Visual Analogue Scale for Pain (VAS-P) assesses subjective perceptions of pain on a scale from 0 to 10, where 0 indicates no pain at all and 10 indicates worst possible pain. Higher scores reflect greater perceived pain.

The Visual Analogue Scale for Pain (VAS-P) assesses subjective perceptions of pain on a scale from 0 to 10, where 0 indicates no pain at all and 10 indicates worst possible pain. Higher scores reflect greater perceived pain.

The Visual Analogue Scale for Pain (VAS-P) assesses subjective perceptions of pain on a scale from 0 to 10, where 0 indicates no pain at all and 10 indicates worst possible pain. Higher scores reflect greater perceived pain.

The Visual Analogue Scale for Pain (VAS-P) assesses subjective perceptions of pain on a scale from 0 to 10, where 0 indicates no pain at all and 10 indicates worst possible pain. Higher scores reflect greater perceived pain.

Muscle oxygen saturation (SMO2) will be measured in both the right and left lateral quadriceps using the Moxy 3-Sensor Bundle (Fortiori Design LLC, Hutchinson, USA), allowing for the calculation of mean SMO2 across the entire training session.

Lactate concentration will be assessed with a lactate analyzer (Lactate Scout system, RedMed, Warsaw, Poland) using fingertip capillary blood samples.

Lactate concentration will be assessed with a lactate analyzer (Lactate Scout system, RedMed, Warsaw, Poland) using fingertip capillary blood samples.

HRV measurements will be taken using a Polar H10 heart rate sensor (Kempele, Finland), which will record heartbeats during sleep. The HRV variables will be analyzed using Kubios HRV software (version 3.0). The Poincaré plot and time and frequency domains will be analyzed.

Serum TSH will be analyzed to assess thyroid function and hormonal regulation. Unit of measure: μIU/mL

Serum levels of IFN-γ will be analyzed to assess pro-inflammatory immune response activity. Unit of measure: pg/mL

Serum levels of IFN-γ will be analyzed to assess pro-inflammatory immune response activity. Unit of measure: pg/mL

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

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

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.

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.

Physical self-perception will be evaluated using the Physical Self-Perception Profile (PSPP), which includes six subscales: sports competence, physical condition, body attractiveness, physical strength, general physical self-perception, and overall self-perception. Each item is rated on a 5-point Likert scale, ranging from 1 (strongly disagree) to 5 (strongly agree). Higher scores indicate more positive self-perceptions in the respective domains.

Pain catastrophizing will be assessed using the Pain Catastrophizing Scale (PCS), which includes 13 items divided into three subscales: rumination, magnification, and helplessness. Participants respond using a 5-point Likert scale, ranging from 0 (not at all) to 4 (all the time). Higher scores indicate greater levels of pain catastrophizing. The total PCS score ranges from 0 to 52.

Quality of life will be assessed using the Multiple Sclerosis Quality of Life-54 (MSQOL-54), a multidimensional health-related quality of life instrument developed specifically for individuals with multiple sclerosis. It includes 14 subscales:

Physical Function (10-100) Role Limitations-Physical (0-100) Role Limitations-Emotional (0-100) Pain (0-100) Emotional Well-being (0-100) Energy (0-100) Health Perceptions (0-100) Social Function (0-100) Cognitive Function (0-100) Health Distress (0-100) Sexual Function (0-100) Sexual Satisfaction (0-100) Change in Health (0-100) Overall Quality of Life (0-100)

The questionnaire also yields two composite summary scores:

Physical Health Composite Score Mental Health Composite Score Each subscale score and composite score ranges from 0 to 100, with higher scores indicating better quality of life.

State and Trait Anxiety will be assessed using the State-Trait Anxiety Inventory (STAI), a widely used instrument developed by Spielberger et al. It consists of two subscales:

State Anxiety (STAI-S) - evaluates how respondents feel "right now, at this moment"

Trait Anxiety (STAI-T) - evaluates how respondents "generally feel"

Each subscale contains 20 items, rated on a 4-point Likert scale:

For STAI-S: from 1 (Not at all) to 4 (Very much so)

For STAI-T: from 1 (Almost never) to 4 (Almost always)

Scores for each subscale range from 20 to 80, with higher scores indicating greater anxiety levels.

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

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

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

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

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

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

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"

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"

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

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

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

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

Tone assessed with MyotonPRO (MyotonPRO, Myoton AS, Estonia). Definition: Oscillation frequency [Hz] that characterizes the intrinsic tension of biological soft tissues at the cellular level.

Tone assessed with MyotonPRO (MyotonPRO, Myoton AS, Estonia). Definition: Oscillation frequency [Hz] that characterizes the intrinsic tension of biological soft tissues at the cellular level.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Participants will be instructed and familiarized with the use of the Borg Rating of Perceived Exertion scale during the familiarization phase. Subjective perception of effort will be assessed before, during (after each exercise within the session), and after the training session using the Borg Rating of Perceived Exertion Scale (6-20 points). On this scale, 6 indicates "no exertion at all" and 20 indicates "maximal exertion". Higher scores represent greater perceived effort.

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

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

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

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.

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.

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.

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.

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.

Body weight will be measured using a calibrated digital scale. The participant will be barefoot and wearing light clothing.

Unit of Measure: Kilograms (kg)

Physical activity will be assessed using the IPAQ (short form), adapted for people with multiple sclerosis. The questionnaire captures frequency and duration of physical activity in walking, moderate, and vigorous domains over the last 7 days. MET values will be adjusted for the functional limitations commonly present in this population. Unit of Measure: MET-minutes per week

Adherence to the Mediterranean Diet will be assessed using the MEDAS (Mediterranean Diet Adherence Screener), a validated 14-item questionnaire designed to evaluate dietary patterns. The questionnaire measures adherence based on the consumption of key food groups associated with the Mediterranean diet. Unit of Measure: Score on the MEDAS questionnaire (range: 0-14; higher scores indicate greater adherence)

Adherence to the Mediterranean Diet will be assessed using the MEDAS (Mediterranean Diet Adherence Screener), a validated 14-item questionnaire designed to evaluate dietary patterns. The questionnaire measures adherence based on the consumption of key food groups associated with the Mediterranean diet. Unit of Measure: Score on the MEDAS questionnaire (range: 0-14; higher scores indicate greater adherence)

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) Time Frame: Before the first session of the intervention program

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) Time Frame: Before the first session of the intervention program

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]).

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]).

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]).

Time Frame: Before the first session of the intervention program

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]).

Time Frame: Before the first session of the intervention program

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]).

Time Frame: Before the first session of the intervention program

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)

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)

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)

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)

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)

Serum progesterone levels will be measured to confirm luteal phase and ovulatory patterns. Unit of measure: ng/mL

LH will be measured to detect the ovulatory surge and determine phase timing. Unit of measure: mIU/mL

FSH levels will be assessed to evaluate ovarian function. Unit of measure: mIU/mL

Serum estradiol will be analyzed to confirm hormonal variation across the menstrual cycle. Unit of measure: pg/mL

Serum testosterone will be measured to examine androgen levels. Unit of measure: ng/dL

Serum IL-6 will be measured to evaluate systemic inflammation. Unit of measure: pg/mL

Serum IL-6 will be measured to evaluate systemic inflammation. Unit of measure: pg/mL

TNF-α levels will be assessed as an indicator of inflammatory status. Unit of measure: pg/mL

TNF-α levels will be assessed as an indicator of inflammatory status. Unit of measure: pg/mL

IL-10 will be measured to evaluate anti-inflammatory responses. Unit of measure: pg/mL

IL-10 will be measured to evaluate anti-inflammatory responses. Unit of measure: pg/mL

TGF-β1 levels will be analyzed as part of the immunomodulatory and regulatory response profile.

Unit of measure: ng/mL

TGF-β1 levels will be analyzed as part of the immunomodulatory and regulatory response profile. Unit of measure: ng/mL

Stiffness assessed with MyotonPRO (MyotonPRO, Myoton AS, Estonia). Definition: dynamic stiffness (N/m) characterizes the resistance of biological soft tissues to a force of deformation

Stiffness assessed with MyotonPRO (MyotonPRO, Myoton AS, Estonia). Definition: dynamic stiffness (N/m) characterizes the resistance of biological soft tissues to a force of deformation

Elasticity assessed with MyotonPRO (MyotonPRO, Myoton AS, Estonia). Definition elasticity: logarithmic decrement (arb) characterizes the dampening of tissue oscillation.

Elasticity assessed with MyotonPRO (MyotonPRO, Myoton AS, Estonia). Definition elasticity: logarithmic decrement (arb) characterizes the dampening of tissue oscillation

Relaxation assessed with MyotonPRO (MyotonPRO, Myoton AS, Estonia). Definition relaxation: Mechanical stress relaxation time (ms) characterizes tissue´s recovery time from displacement.

Relaxation assessed with MyotonPRO (MyotonPRO, Myoton AS, Estonia). Definition relaxation: Mechanical stress relaxation time (ms) characterizes tissue´s recovery time from displacement.

Creep assessed with MyotonPRO (MyotonPRO, Myoton AS, Estonia). Definition creep: ratio of relaxation and deformation time (arb) characterizes creep, the gradual elongation of tissue over time when placed under constant tensile stress.

Creep assessed with MyotonPRO (MyotonPRO, Myoton AS, Estonia). Definition creep: ratio of relaxation and deformation time (arb) characterizes creep, the gradual elongation of tissue over time when placed under constant tensile stress.

Height will be measured using a wall-mounted stadiometer with the participant barefoot and standing upright.

Unit of Measure: Meters (m)

BMI will be calculated as weight in kilograms divided by the square of height in meters (kg/m²). Body weight and height will be assessed using a calibrated digital scale and stadiometer, respectively.

Objective physical activity will be measured using a triaxial accelerometer, which captures movement in three planes (vertical, lateral, and anterior-posterior). Variables include time spent in light, moderate, and vigorous physical activity, as well as step count. This tool enables detailed quantification of low-intensity movements common in individuals with MS. Unit of Measure: Minutes per day in activity categories; steps per day

Dietary intake will be assessed using a 3-day food diary, including two weekdays and one weekend day. Participants will record all food and beverages consumed, and a registered dietitian will analyze macronutrient and micronutrient intake using nutrition software. Unit of Measure: Daily intake in grams (carbohydrates, proteins, fats) and milligrams/micrograms (vitamins, minerals), as appropriate

Dietary intake will be assessed using a 3-day food diary, including two weekdays and one weekend day. Participants will record all food and beverages consumed, and a registered dietitian will analyze macronutrient and micronutrient intake using nutrition software. Unit of Measure: Daily intake in grams (carbohydrates, proteins, fats) and milligrams/micrograms (vitamins, minerals), as appropriate

Lean mass will be evaluated using BIA and DXA, both for the entire body and segmentally (arms, legs, trunk). Unit of Measure: %

Lean mass will be evaluated using BIA and DXA, both for the entire body and segmentally (arms, legs, trunk). Unit of Measure: kilograms

Bone Mineral Content will be measured using DXA, both globally and at specific body segments (e.g., spine, hips, limbs). BMC indicates the total mineral content in bones and is essential for assessing bone health in MS. Unit of Measure: Grams (g)

Bone Mineral Density will be assessed with DXA, capturing whole-body and segmental (lumbar spine, femoral neck, etc.) density in g/cm². BMD reflects bone strength and fracture risk.

Unit of Measure: g/cm²

Total body water will be measured using BIA, evaluating both intracellular and extracellular compartments. Segmental analysis (e.g., limbs and trunk) will also be included to reflect fluid distribution patterns. Unit of Measure: Liters (L)

Phase angle will be assessed with BIA for both total and segmental body regions. It reflects cellular health and membrane integrity, and is an important marker of nutritional and physiological status in MS patients. Unit of Measure: Degrees (°)

HRV measurements will be taken using a Polar H10 heart rate sensor (Kempele, Finland), which participants will be instructed to wear when going to bed. The sensor will record heartbeats during sleep, and the data will be analyzed using Kubios HRV software (version 3.0). The Poincaré plot and time and frequency domains will be analyzed.

HRV measurements will be taken using a Polar H10 heart rate sensor (Kempele, Finland), which participants will be instructed to wear when going to bed. The sensor will record heartbeats during sleep, and the data will be analyzed using Kubios HRV software (version 3.0). The Poincaré plot and time and frequency domains will be analyzed.

HRV measurements will be taken using a Polar H10 heart rate sensor (Kempele, Finland), which participants will be instructed to wear when going to bed. The sensor will record heartbeats during sleep, and the data will be analyzed using Kubios HRV software (version 3.0). The Poincaré plot and time and frequency domains will be analyzed.

HRV measurements will be taken using a Polar H10 heart rate sensor (Kempele, Finland), which participants will be instructed to wear when going to bed. The sensor will record heartbeats during sleep, and the data will be analyzed using Kubios HRV software (version 3.0). The Poincaré plot and time and frequency domains will be analyzed.

Fat mass will be measured using bioelectrical impedance analysis (BIA) and dual-energy X-ray absorptiometry (DXA). Both whole-body and segmental (arms, legs, trunk) fat mass will be assessed. Unit of Measure: Kilograms

Fat mass will be measured using bioelectrical impedance analysis (BIA) and dual-energy X-ray absorptiometry (DXA). Both whole-body and segmental (arms, legs, trunk) fat mass will be assessed. Unit of Measure: %