Temperature-elevating Armbaths for Arterial Hypertension

Sponsor
Kliniken Essen-Mitte (Other)
Overall Status
Recruiting
CT.gov ID
NCT05928702
Collaborator
Karl and Veronica Carstens Foundation (Other)
50
1
2
12.1
4.1

Study Details

Study Description

Brief Summary

The goal of this randomized controlled trial is to learn about the effect of a hydrotherapeutic approach - a temperature-elevating armbath - in people with arterial hypertention. The main question[s] it aims to answer are:

  • Can this kind of hydrotherapy lower the blood pressure and therefore be an additional approach to medical treatment in arterial hypertension?

  • Besides blood pressure regulation, does this intervention affect sleep quality when being performed at night time or does it affect overall quality of life?

Participants will be advised to perform a temperature-elevating armbath once a day for 30 minutes on at least 5 days per week over 8 weeks.

The comparison group will continue treatment as usual, like continue their medication. 24h blood pressure measurements will be performed at the beginning, after 8 weeks and after 6 months in both groups. The main goal is to evaluate whether the intervention group shows lower blood pressure levels after a certain time of treatment.

After 6 months (end of trial) the control group will be offered to learn the temperature elevating armbath as well.

Condition or Disease Intervention/Treatment Phase
  • Procedure: temperature-elevating armbath
N/A

Detailed Description

Arterial hypertension remains one of the most important risk factors in developing a cardiovascular disease. While medical treatment is usually necessary, lifestyle modifications should always be included. Besides physical activity and a balanced diet, there are also therapeutic approaches from the so called classical complementary medicine. One very important part in Europe is hydrotherapy, based on ideas of Sebastian Kneipp and his contemporaries. In hydrotherapy there are various therapeutic approaches that can be used additionally to conventional therapy. Because conventional medical therapy is often associated with unwanted side effects, these additional approaches experience increasing popularity. In arterial hypertension, temperature-elevating armbaths, developed by Kneipps contemporaries Hauffe and Schwenninger, are a hydrotherapeutic approach that is highly recommended. Even though hydrotherapy has been a part of complementary medicine for more than a century now some therapeutic approaches lack of scientific evidence - especially when it comes to their effect on arterial hypertension.

This randomized-controlled trial aims to evaluate the effect of a temperature-elevating armbath among participants with arterial hypertension. 50 participants will be randomized to either an intervention group or waitlist (treatment as usual). All 50 participants will be monitored with three 24-hours ambulatory blood pressure measurements (24h ABPM) at the beginning of the trial after randomization, at 8 weeks and at 6 months.

The intervention group will be advised to perform the armbaths on 5 of 7 days per week for 8 weeks total. Each participant will get a detailed instruction how to perform the armbath and will be handed a diary to document their performance.

After 6 months, each participant of the control group will be offered to be instructed on performing the armbaths as well.

Within the active period of 8 weeks, participants of both groups will be called regularly to ask about their health and whether they have questions regarding the trial.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
randomized controlled trialrandomized controlled trial
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
The Effect of Temperature-elevating Armbaths (Hauffe-Schwenniger-Baths) as a Therapeutic Option to Regulate the Blood Pressure in People With Arterial Hypertension - a Randomized-controlled Trial (Wirksamkeit Temperaturansteigender Armbäder (Hauffe-Schweninger Bäder) Zur Regulierung Des Blutdrucks Bei Probanden Mit Arterieller Hypertonie - Eine Randomisiert-kontrollierte Studie)
Actual Study Start Date :
Jun 23, 2023
Anticipated Primary Completion Date :
Dec 23, 2023
Anticipated Study Completion Date :
Jun 24, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Armbath

The armbath group will perform a temperature-elevating armbath developed by Hauffe and Schwenninger. A large bowl and a thermometer will be given to each participant. Participant start with bathing their forearms up to about one third of the upper arm in a large bowl with water at approximately 37°C. Within 30min, they are advised to add hot water to the bowl for multiple times until a temperature of 42°C. After 30min, the arms can be taken out of the water, dried, and participants are recommended to rest for additional 30 min afterwards. Prior medication should be continued throughout the whole trial.

Procedure: temperature-elevating armbath
Hydrotherapeutic Approach

No Intervention: Waitlist

Participants will continue their treatment as usual (e.g. medication). After the end of the trial (6 months) they will be offered to get instructed on performing temperature-elevating armbaths.

Outcome Measures

Primary Outcome Measures

  1. Blood pressure [to 8 weeks]

Secondary Outcome Measures

  1. Blood pressure [to 6 months]

  2. SF-12 [to 8 weeks and 6 months]

    Health-related quality of life

  3. PSQI [to 8 weeks and 6 months]

    Sleep quality

  4. heartrate [to 8 weeks and 6 months]

  5. Adverse events [to 8 weeks and 6 months]

  6. Medication [to 8 weeks and 6 months]

    Monitoring of changes in medication

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • adult participants (≥18 years)

  • diagnosed arterial hypertension, at least stage I, based on the Guidelines of the European Society of Hypertension 2018 (systolic >140 mmHg, diastolic >90 mmHg)

  • last change in medication at least 2 months ago

  • no planned changes in blood pressure medication within intervention time; changes due to medical reasons (e.g., hypotension, hypertensive emergency) are allowed.

  • willingness to perform an armbath on a regular schedule (min. 5x/weeks)

Exclusion Criteria:
  • acute psychiatric disease ( e.g., addiction, major depression)

  • acute or major physical disease (e.g., cancer diagnosis within the last 5 years, major known cardiovascular diseases, renal or liver dysfunction), acute infection, major neurological diseases (e.g., Parkinsons´ disease, uncontrolled epilepsy)

  • secondary hypertension

  • pregnancy or lactation period

Contacts and Locations

Locations

Site City State Country Postal Code
1 Kliniken Essen-Mitte Essen North-Rhine-Westphalia Germany 45276

Sponsors and Collaborators

  • Kliniken Essen-Mitte
  • Karl and Veronica Carstens Foundation

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Kohl, Wiebke, MD, Kliniken Essen-Mitte
ClinicalTrials.gov Identifier:
NCT05928702
Other Study ID Numbers:
  • WKHypertension
First Posted:
Jul 3, 2023
Last Update Posted:
Jul 3, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Kohl, Wiebke, MD, Kliniken Essen-Mitte
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 3, 2023