The Effectiveness of the Wim Hof Method

Sponsor
University of Bern (Other)
Overall Status
Completed
CT.gov ID
NCT05894031
Collaborator
(none)
42
1
2
5
8.4

Study Details

Study Description

Brief Summary

The Wim Hof Method is a multi-disciplinary approach to physical and mental well-being combining cold exposure, breathing exercises, and meditation. This study evaluated the effects of a 15-day WHM intervention on cardiovascular parameters at rest and during a cold pressor test, as well as on various psychological parameters.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Wim Hof Method
N/A

Detailed Description

The Wim Hof Method (WHM) is a multi-disciplinary approach to physical and mental well-being combining cold exposure, breathing exercises, and meditation. This study evaluated the effects of a 15-day WHM intervention on cardiovascular parameters at rest and during a cold pressor test (CPT), as well as on various psychological parameters.

42 participants were randomized into an intervention (IG) and a control (CG) group. Throughout the 15-day intervention, the IG performed the WHM daily. The intervention followed the guidelines provided by Wim Hof. The intervention comprised three components: cold water exposure, breathing exercise, and meditation. The participants were instructed to perform the WHM daily over the course of 15 days. The participants could choose when to do so throughout the day, however, the components were to be performed in a strict, sequential order: breathing exercises, followed by meditation, and then cold exposure. Participants were asked to complete a daily log in which they documented whether they performed the procedure and for how long. Altogether, the procedure lasted about 15 minutes. The CG did not receive an intervention throughout the intervention period.

Before and after the intervention, systolic (SBP) and diastolic blood pressure (DBP), pulse wave velocity (PWV), heart rate (HR), root mean sum of squared distance (RMSSD), and standard deviation of intervals between successive heartbeats (SDNN) were assessed at rest and during a CPT. Furthermore, perceived stress (PSS), positive affect (PANAS+), negative affect (PANAS-), and subjective vitality (trait (SVSt) and state (SVSs)) was determined.

Study Design

Study Type:
Interventional
Actual Enrollment :
42 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Randomized controlled trial with parallel armsRandomized controlled trial with parallel arms
Masking:
Single (Outcomes Assessor)
Masking Description:
Blinding of outcome assessors
Primary Purpose:
Prevention
Official Title:
The Effectiveness of the Wim Hof Method on Cardiac Autonomic Function, Blood Pressure, Arterial Compliance, and Different Psychological Parameters
Actual Study Start Date :
May 1, 2022
Actual Primary Completion Date :
Jul 30, 2022
Actual Study Completion Date :
Sep 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

The intervention group was instructed to perform the Wim Hof Method daily over the course of 15 days. The participants could choose when to do so throughout the day, however, the components were to be performed in a strict, sequential order: breathing exercises, followed by meditation, and then cold exposure. Participants were asked to complete a daily log in which they documented whether they performed the procedure and for how long. Altogether, the procedure lasted about 15 minutes.

Behavioral: Wim Hof Method
The intervention followed the guidelines provided by Wim Hof. The intervention comprised three components: cold water exposure, breathing exercise, and meditation.The participants were instructed to perform the WHM daily over the course of 15 days. The participants could choose when to do so throughout the day, however, the components were to be performed in a strict, sequential order: breathing exercises, followed by meditation, and then cold exposure. Participants were asked to complete a daily log in which they documented whether they performed the procedure and for how long. Altogether, the procedure lasted about 15 minutes.

No Intervention: Control

The control group received noch intervention throughout the intervention period.

Outcome Measures

Primary Outcome Measures

  1. Change from baseline in the mean systolic blood pressure [15 days]

    Participants were instructed to rest in a supine position for 10 minutes prior to the measurement. At least two readings were taken on the right upper arm, using custom-fitted arm cuffs.

  2. Change from baseline in the mean diastolic blood pressure [15 days]

    Participants were instructed to rest in a supine position for 10 minutes prior to the measurement. At least two readings were taken on the right upper arm, using custom-fitted arm cuffs.

Secondary Outcome Measures

  1. Change from baseline in the mean pulse wave velocity [15 days]

    Participants were instructed to rest in a supine position for 10 minutes prior to the measurement. At least two readings were taken on the right upper arm, using custom-fitted arm cuffs.

  2. Change from baseline in the mean heart rate variability [15 days]

    Heart rate variability (HRV) was measured using a heart rate monitor and chest strap. Participants were instructed to empty their bladder before the measurement, which was conducted after a 5-minute supine rest period with a stabilized HRV signal. The measurement consisted of a 5-minute recording of intervals between successive heartbeats at a 1000 Hz sampling rate. Participants were instructed to breathe normally, remain quiet, and maintain a calm state throughout the measurement.

  3. Change from baseline in positive affect [15 days]

    The German version of the Positive and Negative Affect Schedule was used.

  4. Change from baseline in negative affect [15 days]

    The German version of the Positive and Negative Affect Schedule was used.

  5. Change in subjective vitality [15 days]

    The German 6-item Version of the Subjective Vitality Scale was used.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Being male

  • No underlying health conditions

  • Not using antihypertensive or other cardiovascular medications

  • Not engaging in regular exercise training

  • Written informed consent

Exclusion Criteria:
  • Having prior experience with any of the components of the intervention (breathing, meditation, or cold exposure)

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Bern Bern Switzerland 3012

Sponsors and Collaborators

  • University of Bern

Investigators

  • Principal Investigator: Sascha Ketelhut, PhD, University of Bern

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Bern
ClinicalTrials.gov Identifier:
NCT05894031
Other Study ID Numbers:
  • 2022-04-00004
First Posted:
Jun 8, 2023
Last Update Posted:
Jun 8, 2023
Last Verified:
May 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Bern

Study Results

No Results Posted as of Jun 8, 2023