Skip to main content
OpenTrials
Completed

NCT Number: NCT06248281

Be Cool: An Innovative and Holistic Psychoeducational Program for Multiple Sclerosis Individuals

This observational study aims to investigate the impact of an online psychoeducational program, combined with cooling therapy, nutrition, psychological intervention, and exercise, on the resilience, treatment adherence, symptom management, and quality of life of individuals with Multiple Sclerosis. The study will last for six months, during which two groups of 15 participants with similar characteristics and a diagnosis of Multiple Sclerosis will take part in the protocol. Group A will follow the research protocol, while Group B, the Control group, will not participate in any rehabilitation intervention.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Multiple Sclerosis Autoimmune Diseases Autoimmune Diseases of the Nervous System Demyelinating Autoimmune Diseases, CNS Demyelinating Diseases Immune System Diseases Nervous System Diseases

Age range

19 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Greek Multiple Sclerosis Society

Thessaloniki, Central Macedonia, 55132, Greece

About this study

Fifteen individuals with multiple sclerosis will participate in an innovative, hybrid rehabilitation program, encompassing several key components to enhance their well-being. The program includes:

  • Exercise Intervention: Participants will engage in specially designed exercise programs. Every two weeks, they will meet virtually with an exercise physiologist via Microsoft Teams for tailored education about their specific needs. Additionally, a customized exercise video will be uploaded weekly to the Teams platform, ensuring ongoing physical engagement.
  • Nutritional Evaluation and Education: Nutrition is a core focus. A nutritionist will meet with the participants bi-weekly to discuss their dietary needs and educate them on maintaining a balanced diet to support their condition. Further enhancing this aspect, a nutritious recipe will be uploaded to the platform each week, offering practical dietary guidance.
  • Psychological Support: Psychological well-being is addressed through weekly group meetings conducted by a psychologist. These sessions will utilize Acceptance and Commitment Therapy (ACT) strategies to help participants manage their symptoms, accept their condition, and improve their overall quality of life.
  • Head and Neck Cooling Strategy: Recognizing the importance of temperature regulation in MS, participants will be advised to apply a cooling strategy to the head and neck area for at least two hours daily, providing symptomatic relief.

To monitor progress and adjust the program as needed, participants' functional ability, nutritional status, psychological condition, and overall quality of life will be evaluated at three key points: baseline (before starting the program), at the three-month mark, and upon completion of the program at six months.

This program is structured to provide a holistic, supportive, and adaptable approach to managing multiple sclerosis, focusing on physical health, nutritional balance, psychological support, and practical strategies for daily living.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participants must have been diagnosed with MS using the McDonald criteria, ensuring a standardized and validated diagnostic approach.
  • Participants should have been relapse-free during the six months leading up to the study to avoid potential confounding factors.
  • Participants must have no musculoskeletal impediment that could affect their ability to engage in the exercise component of the program.
  • Participants must have a score on the Expanded Disability Status Scale (EDSS) ranging from 0 to 5.5, indicating ambulatory ability without the need for a cane for at least 100 meters.
  • Participants should have a history of sensitivity to heat, as reported by their treating physician, justifying the need for cooling therapy as part of the hybrid program.
  • Participants must not have used cooling therapy or participated in any form of exercise training for at least four months prior to their participation in the study.

-

Exclusion criteria

  • Previously diagnosed conditions known to impact physiological responses to heat exposure, including diabetes mellitus, hypertension, heart disease, or kidney disease.
  • Use of medications to manage MS-related symptoms, such as antidepressants, psychostimulants, anticonvulsants, antispasmodics, and anticholinergic drugs.

-

Treatment and study plan

combination of different rehabilitation strategies

Other

The psychoeducational program will be conducted through weekly online video-conferencing group sessions that will last for two hours. In addition to these sessions, participants will receive psychoeducational material such as readings, videos, podcasts, worksheets, and homework exercises every week. This material will allow participants to practice at their own pace during the session intervals.

The exercise training program for individuals with MS will be tailored to meet the unique and individual needs of each participant. To achieve this, a head and neck cooling protocol will be implemented using commercially available cooling equipment, specifically the Headcool Power and Neckcool Tie from Inuteq. Participants will need to wear the cooling cup and neck wrap for two hours daily. The equipment will be activated using 10°C tap water. Finally, a nutritionist will provide personalized nutritional guidance including weekly diet observation and recipe videos.

Other names: cooling therapy, diet, phycology-behavioral-mindfulness intervention, exercise traiining

Primary outcomes

  1. anxiety and depression

    Time frame: Baseline, after three months and at the end of the six months

    This will be estimated with the "The Hospital Anxiety and Depression Scale - HADS". The Hospital Anxiety and Depression Scale (HADS) is a widely used questionnaire specifically designed to identify and measure the levels of anxiety and depression in individuals. It is particularly useful in medical settings, as it helps distinguish between psychological distress and physical illness.

  2. Overall quality of life, namely satisfaction with their life

    Time frame: Baseline, after three months and at the end of the six months

    This will be estimated with the questionnaire of Multiple Sclerosis Quality of Life-54 (MSQOL-54)

  3. Perception of stress

    Time frame: Baseline, after three months and at the end of the six months

    Perceived Stress Scale (PSS) will be used. This is a widely used psychological instrument for measuring the perception of stress. It assesses the degree to which situations in one's life are appraised as stressful. Items on the PSS ask about feelings and thoughts during the last month, and scores on the PSS can range from 0 to 40, with higher scores indicating higher perceived stress.

  4. Cognitive fusion which refers to the degree to which an individual's thoughts and feelings are intertwined with their sense of self, often leading to an inability to separate from, or 'defuse' from, these internal experiences.

    Time frame: Baseline, after three months and at the end of the six months

    The Cognitive Fusion Questionnaire (CFQ-7) questionnaire that measures cognitive fusion, which a key concept in Acceptance and Commitment Therapy (ACT) will be used. The CFQ-7, with its 7 items, assesses the extent to which a person experiences this phenomenon.

  5. The value of living

    Time frame: Baseline, after three months and at the end of the six months

    The Valued Living Questionnaire (VLQ) will be used. The VLQ is designed to assess valued living, which is another core concept in ACT. It helps individuals to identify what is truly important and meaningful to them in various domains of life (such as family, career, health) and to what extent they have been living in accordance with these values.

  6. Psychological flexibility which is the ability to be in the present moment with full awareness and openness to experiences, and to take action guided by one's values.

    Time frame: Baseline, after three months and at the end of the six months

    The MPFI-Psychological Flexibility Subscale will be used. This subscale is part of a larger questionnaire and specifically measures psychological flexibility, an essential aspect of mental health and well-being.

  7. The resilience which is defined as the ability to cope with and bounce back from adversity.

    Time frame: Baseline, after three months and at the end of the six months

    The Connor-Davidson Resilience Scale (CDRISC-25) will be used. This 25-item scale measures resilience, defined as the ability to cope with and bounce back from adversity. Higher scores indicate greater resilience.

  8. Aerobic capacity and ability to walk

    Time frame: Baseline, after three months and at the end of the six months

    The Two Minute Walk Test (2MWT) is a simple, easy-to-administer functional exercise test used primarily in clinical settings. It measures the distance an individual is able to walk on a flat, hard surface in a period of two minutes.

  9. Lower body strength and functional mobility

    Time frame: Baseline, after three months and at the end of the six months

    The Five Times Sit to Stand Test (5xSST) will be used which is a simple yet effective physical performance test used primarily to assess lower body strength and functional mobility. The test involves timing how long it takes an individual to stand up and sit down five times as quickly as possible from a standard height chair without using their arms for support. A longer time to complete the test generally indicates lower functional performance.

  10. Static and dynamic balance ability

    Time frame: Baseline, after three months and at the end of the six months

    The Berg Balance Scale (BBS) will be used which is a widely used clinical test of a person's static and dynamic balance abilities. It is particularly common in elderly populations and among those recovering from injury or dealing with conditions that affect balance.

  11. Mobility and walking speed

    Time frame: Baseline, after three months and at the end of the six months

    The Timed 25-Foot Walk (T25-FW) will be used which is a functional test commonly used to assess mobility and walking speed in individuals, particularly those with neurological conditions such as multiple sclerosis (MS).The test involves timing how quickly a person can walk 25 feet at their usual pace, usually conducted along a flat, straight course.

Secondary outcomes

  1. Finger dexterity and arm-hand coordination

    Time frame: Baseline, after three months and at the end of the six months

    The 9-Hole Peg Test (9-HPT) will be used which is a standardized, widely used assessment tool in clinical and research settings to measure finger dexterity and arm-hand coordination. It's particularly useful for evaluating upper extremity function in individuals with neurological conditions, such as multiple sclerosis (MS) and stroke.

  2. Core temperature

    Time frame: Baseline, after three months and at the end of the six months

    With a gastrointestinal telemetric capsule (e-Celsius)

  3. Skin temperature

    Time frame: Baseline, after three months and at the end of the six months

    iButtons

  4. Nutritional status, how balance is their nutrition

    Time frame: Baseline, after three months and at the end of the six months

    This will be estimated with questionnaires

Sponsors and collaborators

Lead sponsor

University of Thessaly

Other

Collaborators

  • European Committee for Treatment and Research in Multiple Sclerosis
  • Greek Multiple Sclerosis Society

Registry information

Official study title

Be Cool: An Innovative and Holistic Psychoeducational Program to Improve and Promote Care, Education and Quality of Life for Multiple Sclerosis Individuals

Acronym: BeCool

Important dates

Study start
2023
Primary completion
2023
Study completion
2024
First posted
Feb 8, 2024
Registry last updated
May 8, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.