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Clinical Trials/NCT05704322
NCT05704322CompletedNot Applicable

The Effectiveness of the Wim Hof Method on Physical and Mental Health of People with a Spinal Cord Injury

Stichting Reade2 sites in 1 country60 target enrollmentStarted: March 27, 2023Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
60
Locations
2
Primary Endpoint
Change in mental health

Study Overview

Brief Summary

People with a spinal cord injury (SCI) often experience secondary medical complications. One of the methods that may help to prevent or deal with secondary complications in people with SCI is the Wim Hof Method (WHM). The WHM is based on three elements: 1) breathing exercises, 2) gradual cold exposure (cold showers, or cold water immersion), and 3) mindset. The primary objective of this randomized controlled trial is to assess the effects of WHM, involving breathing exercises, mindset (and cold exposure), on health-related quality of life in people with SCI. The secondary objectives are to assess the effects of WHM, involving breathing exercises, mindset (and cold exposure) in people with SCI on: inflammation markers, metabolic health, pulmonary function, body composition, sleep quality, spasticity, stress, and on chronic pain.

Detailed Description

A spinal cord injury (SCI) is a serious medical condition that causes functional, psychological and socioeconomic disorder. Long-term, secondary medical complications are common and play an important role in the continuum of care for people with SCI. Complications are a frequent cause of morbidity and mortality and lead to increased rates of rehospitalisation, loss of employability and decreased quality of life. During multidisciplinary SCI rehabilitation, the treatment is focussed on working with the patient physically and psychologically to maximize their neurological recovery and general health but also to prevent or deal with the secondary complications. One of the methods that may help to prevent or deal with secondary complications in people with SCI is the Wim Hof Method (WHM). The WHM is based on three elements: 1) breathing exercises, 2) gradual cold exposure (cold showers, or cold water immersion), and 3) mindset. Previous studies showed a positive effect of the WHM on health-related quality of life and the inflammatory profile of healthy individuals as well as patients with active axial spondyloarthritis. Furthermore, a pilot study in people with SCI showed that the WHM (only breathing exercises and mindset) led to positive changes in respiratory function, mental health index, hyperventilation and a trend was visible regarding the hindrance due to spasticity. Some of the participants mentioned that they experienced positive effects on coughing, energy level, mood or used less spasticity medication after the WHM intervention. These positive findings in the pilot study warrant a full-scale randomised-controlled trial (RCT) of this novel therapeutic approach in people with SCI.

The primary objective of this randomized controlled trial is to assess the effects of WHM, involving breathing exercises, mindset (and cold exposure), on health-related quality of life in people with SCI. The secondary objectives are to assess the effects of WHM, involving breathing exercises, mindset (and cold exposure) in people with SCI on: inflammation markers, metabolic health, pulmonary function, body composition, sleep quality, spasticity, stress, and on chronic pain.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Individuals (Male/Female) with either a complete or incomplete chronic SCI. In this study, a chronic SCI is defined as a time since injury ≥ 1 year.
  • Participants have to be between 18 and 75 years old.

Exclusion Criteria

  • Cardiac arrhythmias or cardiac disease;
  • A history of severe autonomic dysreflexia assessed with the 'Autonomic standards assessment';
  • Severe pulmonary disease (such as COPD) based on a pulmonary history;
  • Insufficient mastery of the Dutch language (speaking and reading);
  • Severe cognitive or communicative disorders;
  • Progressive disease;
  • Being or becoming pregnant during the study period;
  • Severe psychiatric illness or disorders (at the discretion of the treating rehabilitation physician);
  • Involved in another intervention study which may have an effect on the outcome measures of the present study;
  • Experience with (parts of) the Wim Hof Method.
  • Negative advice from physician to participate in the Wim Hof Method intervention based on the medical screening.

Outcomes

Primary Outcomes

Change in mental health

Time Frame: Assessed before and after the 7-weeks WHM intervention

Mental Health Index - 5 (MHI-5), a subscale of the SF-36. The MHI-5 has a score of 0 to 100, where a score of 100 represents optimal mental health.

Secondary Outcomes

  • Change in CRP(Assessed before and after the 7-weeks WHM intervention)
  • Change in mindful attention awareness(Assessed before and after the 7-weeks WHM intervention)
  • Change in hyperventilation(Assessed before and after the 7-weeks WHM intervention)
  • Change in high-density lipoprotein(Assessed before and after the 7-weeks WHM intervention)
  • Change in total cholesterol(Assessed before and after the 7-weeks WHM intervention)
  • Change in forced vital capacity(Assessed before and after the 7-weeks WHM intervention)
  • Change in forced inspiratory volume(Assessed before and after the 7-weeks WHM intervention)
  • Change in sleep quality(Assessed before and after the 7-weeks WHM intervention)
  • Change in fasted glucose(Assessed before and after the 7-weeks WHM intervention)
  • Change in low-density lipoprotein(Assessed before and after the 7-weeks WHM intervention)
  • Change in forced expiratory volume(Assessed before and after the 7-weeks WHM intervention)
  • Change in peak expiratory flow(Assessed before and after the 7-weeks WHM intervention)
  • Change in health-related quality of life(Assessed before and after the 7-weeks WHM intervention)
  • Change in pain and pain interference(Assessed before and after the 7-weeks WHM intervention)
  • Change in hindrance due to spasticity(Assessed before and after the 7-weeks WHM intervention)
  • Change in IL-6(Assessed before and after the 7-weeks WHM intervention)
  • Change in triglycerides(Assessed before and after the 7-weeks WHM intervention)
  • Change in blood pressure(Assessed before and after the 7-weeks WHM intervention)
  • Participant compliance and experiences(Assessed before and after the 7-weeks WHM intervention)
  • Change in peak inspiratory flow(Assessed before and after the 7-weeks WHM intervention)
  • Change in body mass(Assessed before and after the 7-weeks WHM intervention)
  • Change in fat and fat free mass(Assessed before and after the 7-weeks WHM intervention)

Investigators

Sponsor
Stichting Reade
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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