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Effects of Head and Neck Cooling and Heating on Fatigue in Multiple Sclerosis and Healthy Men

Not Applicable
Completed
Conditions
Multiple Sclerosis
Interventions
Other: Heating of the head and neck
Other: Cooling of the head and neck
Registration Number
NCT06370403
Lead Sponsor
Lithuanian Sports University
Brief Summary

Local head and neck cooling strategies can help reduce multiple sclerosis-related fatigue, while heating can exacerbate heat-related fatigue. However, no study has detailed the peripheral and central responses to head and neck cooling (at 18°C) and heating (at 43 ± 1°C next to the scalp and neck skin) during fatiguing isometric exercise in non-challenging ambient temperature in multiple sclerosis and healthy male subjects. In addition, there is a lack of data describing the effects of head and neck cooling/heating and strenuous exercise on blood markers, muscle temperature, motor accuracy, and rate of perceived exertion. The investigators hypothesized that: (i) men with multiple sclerosis would be more affected by central and peripheral fatigue compared to healthy subjects; (ii) local cooling will result in greater central fatigue but will be associated with greater peripheral fatigue, whereas heating will result in greater central and peripheral fatigue in multiple sclerosis men; (iv) local cooling and heating will have a greater effect on the release of stress hormones, rate of perceived exertion and motor accuracy compared to the control condition in both multiple sclerosis and healthy groups.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
40
Inclusion Criteria

Not provided

Exclusion Criteria
  • Physical limitations that would impair the ability to perform neuromuscular testing
  • Mental disorders, such as depression or anxiety, due to their recognized association with fatigue
  • Involvement in temperature manipulation program for ≥ 3 months
  • Attending any excessive physical exercise or sports programs
  • With blood/needle phobia

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Heating of the head and neck in multiple sclerosis and healthy subjectsHeating of the head and neckMultiple sclerosis and healthy male subjects participated in the head and heating program. During heating procedure, the participant performed fatiguing isometric motor task with a head and neck heating helmet at (43°C± 1°C next to the head and neck skin).
Cooling of the head and neck in multiple sclerosis and healthy subjectsCooling of the head and neckMultiple sclerosis and healthy male subjects participated in the head and neck cooling program. During cooling procedure, the participant performed fatiguing isometric motor task with a head and neck cooling helmet at (18°C next to the head and neck skin).
Primary Outcome Measures
NameTimeMethod
Body mass index (kg/m2)Every time in all conditions at the baseline

The body mass index (in kg/m2) was defined as the body mass divided by the square of the body height.

Body fat (%)Every time in all conditions at the baseline

Body fat (%) was assessed using Tanita Body Composition Analyzer (Japan).

Body free fat mass (kg)Every time in all conditions at the baseline

Body free fat mass (kg) was evaluated using Tanita Body Composition Analyzer (Japan).

Change in muscle temperature (°C)Baseline, up to 60 minutes, up to 120 minutes, after 180minutes

Muscle temperature was measured using a needle microprobe (Intramuscular Probe MKA, thermometer model DM-852, Ellab) inserted approximately 3 cm beneath the skin surface into the vastus lateralis muscle of the right leg.

Change in plasma cortisol (nmol/L) concentrationsBaseline, up to 60 minutes, up to 120 minutes, after 180minutes

Plasma cortisol concentrations (nmol/L) were measured using an AIA-2000 automated enzyme immunoassay analyser (Tosoh Corp, Tokyo, Japan).

Change in plasma dopamine (nmol/L) concentrationsBaseline, up to 60 minutes, up to 120 minutes, after 180minutes

Dopamine concentrations (nmol/L) were measured using a kit for dopamine enzyme-linked immunosorbent assay (ELISA) (IBL, Hamburg, Germany).

Change in plasma prolactin (ng/mL) concentrationsBaseline, up to 60 minutes, up to 120 minutes, after 180minutes

Prolactin levels (ng/mL) were measured using a kit for prolactin ELISA (IBL) and Gemini analyzer (Stratec Biomedical GmbH, Germany).

Body weight (kg)Every time in all conditions at the baseline

Body weight (kg) was evaluated using Tanita Body Composition Analyzer (Japan).

Change in involuntary torque (Nm)Baseline, up to 60 minutes, up to 120 minutes, after 180minutes

Involuntary torque of the quadriceps muscles were measured using an isokinetic dynamometer (Biodex Medical Systems, USA) and a high-voltage stimulator (Digitimer DS7A, Digitimer, UK). Peak torques (in Nm) induced by electrical stimulation at 20 Hz,at 100 Hz, and at TT100 were measured.

Change in muscle contraction and relaxation (ms)Baseline, up to 60 minutes, up to 120 minutes, after 180minutes

The contraction and half-relaxation time (in ms) were measured in 100Hz stimulated contractions.

Change in central activation ratio (percent)Baseline, up to 60 minutes, up to 120 minutes, after 180minutes

To evaluate central activation ratio (CAR), a TT-100 Hz stimuli was superimposed on the maximal voluntary contraction (MVC), and the CAR was computed using the following equation: CAR = MVC/(MVC+TT-100 Hz) × 100percent, where where a CAR of 100 percent indicates complete activation of the exercising muscle and a CAR \< 100 percent indicates central activation failure or inhibition.

Change in muscle activity (Hz)Baseline, up to 60 minutes, up to 120 minutes, after 180minutes

Vastus medialis and vastus lateralis muscles electromyographic (EMG) frequency (in Hz) parameters of muscular activity were measured using surface EMG (Biometrics, UK) thorough neuromuscular function assessment.

Change in constant errorBaseline, up to 60 minutes, up to 120 minutes, after 180minutes

The accuracy of the intermittent isometric contraction tasks was calculated as a constant error. Constant error = ∑(xi - T)/n where xi is the motor task performed (N·m); T is the target quantity, i.e., the motor task required; n is the number of trials; and Σ indicates the mean that was calculated considering the algebraic symbols (±).

Change in muscle activity (mV)Baseline, up to 60 minutes, up to 120 minutes, after 180minutes

Vastus medialis and vastus lateralis electromyographic (EMG) amplitude (in mV) parameters of muscular activity were measured using surface EMG (Biometrics, UK) thorough neuromuscular function assessment.

Change in subjective rating of perceived exertionBaseline, up to 60 minutes, up to 120 minutes, after 180minutes

Perceived exertion was assessed using the Borg scale, ranging from 6 (no exertion) to 20 (maximum exertion).

Change in voluntary torque (Nm)Baseline, up to 60 minutes, up to 120 minutes, after 180minutes

Isometric and isokinetic voluntary torques (in Nm) of the quadriceps muscles were measured using an isokinetic dynamometer (Biodex Medical Systems, USA).

Change in absolute errorBaseline, up to 60 minutes, up to 120 minutes, after 180minutes

The absolute error specifies the absolute deviation from the required target force. Absolute error = ∑\|xi - T\|/n where xi is the motor task performed (N·m); T is the target quantity, i.e., the motor task required; n is the number of trials; and vertical brackets Σ \| \| indicate the mean that was calculated without considering the algebraic symbols (±).

Secondary Outcome Measures
NameTimeMethod
Height (m)Every time in all conditions at the baseline

Height (in m) was measured using a Harpenden anthropometer set (Holtain Ltd, UK)

Trial Locations

Locations (1)

Lithuanian Sports University

🇱🇹

Kaunas, Lithuania

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