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CompletedNCT02200926Updated Sep 12, 2016

Non-pharmacological Treatment for Essential Isolated Systolic Hypertension in Elderly

An interventional study of Loaded breathing training and Unloaded breathing training in Systolic Essential Hypertension, sponsored by Khon Kaen University. Completed at 1 site in Thailand. Open to participants aged 60 Years to 85 Years. Per ClinicalTrials.gov, last updated 2016-09-12.

Sponsored by Khon Kaen University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
60 Years to 85 Years
Sex
All
01

Study summary

The previous studies used the slow loaded breathing device for breathing training (Jones et al., 2010). It has been shown that slow loaded breathing training can reduce resting blood pressure and heart rate in essential hypertensive patients. However, this has not been studied in elderly with essential isolated systolic hypertensive patients. Not only highest prevalence of hypertension in Thailand was found in elderly but also physiological changes in the elderly are cause of interest in this special population. It has many advantages to use a slow loaded breathing training in elderly people. Firstly, it is low technology and easily implemented at home. Secondly, it can be practiced almost anytime and anywhere. Thirdly, the orthopedic complications of slow loaded breathing training are minimal. Finally, slow loaded breathing training may be enhancing cardiopulmonary function and other fitness traits, but it out of scope of this study. Moreover, slow loaded breathing exercise by itself should not result in any metabolic adaptation of skeletal muscles, such as the forearm, which had not been trained. If slow loaded breathing training modified some central component of the pressor reflex pathway in a way that single muscle training might work, as suggested above, then loaded breathing training would have a modulating effect on the pressor responses of muscles that had not been trained.

We, therefore, aim to study the effect of slow loaded breathing training by using Breathmax on blood pressure at rest and exercise in elderly with essential isolated systolic hypertension and also investigate the autonomic function and others that may be involved with the changed blood pressure in elderly with essential isolated systolic hypertension. We hypothesized that slow loaded and unloaded breathing training could reduce resting and exercising blood pressure in elderly with essential isolated systolic hypertension.

Read the detailed description

All subjects will be trained for blood pressure and heart rate measurement at home by using a digital arm blood pressure monitoring for 2 weeks control periods before start breathing training. After 2 weeks, subjects in both breathing training groups will trained to inspire deeply against the resistance setting by using Breathmax at the loaded of 18 centimeter of water (cmH2O) and 0 cmH2O (no resistance) with breathing frequency control at 6 breaths/minute in loaded breathing (LB) and unloaded breathing (ULB) group, respectively. They will rest for 5 seconds after every 6 deep breathing. Breathing pattern will be controlled at duty cycle of 0.4 (inspiratory time = 4 sec and total respiratory time = 10 sec). The paced breathing will be practice using metronome at the laboratory until the subjects can do independently without metronome. The breathing was performed normally in control groups (C). The training program will be performed at home for 30 minutes/day, 7 days/week for 8 weeks.

After 8 weeks of breathing training, the sustainability of breathing training effect will be assessed. Subjects in both breathing training groups (LB and ULB) will be stop breathing training with Breathmax and change to breathing normally. In contrast with the subjects in control group, they will be divided to 2 subgroups. The first subgroup performed loaded breathing training at the loaded of 18 cmH2O. The another subgroup performed unloaded breathing training at the loaded of 0 cmH2O. Breathing frequency will be control at 6 breaths/minute in both subgroups. The training program will be performed at home for 30 minutes/day, 7 days/week for 8 weeks.

Data collection will be carried out for 4 times: (1) before control, (2) before training, (3) after training and (4) after stop training. All measurement will be done in the cardiovascular laboratory room, department of physical therapy, faculty of associated medical sciences. In addition, self measurement of blood pressure and heart rate will be conducted at home every morning after getting up at the same time throughout the study (from week 0 to 18).

02

Conditions studied

  • Systolic Essential Hypertension
03

In context

Hypertension

6,690 studies on the registry are indexed under Hypertension; 966 are open to participants now.

This study's enrollment of 30 is below the median of 90 across 4,996 interventional studies indexed under Hypertension.

Browse Hypertension studies →

Lead sponsor

Khon Kaen University is the lead sponsor of 160 studies on the registry; 24 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
60 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Essential isolated systolic hypertension (stage I- II, based on recommendations of JNC-VII)
  • Good communication

Exclusion criteria

Exclusion Criteria:

  • Essential hypertension stage III or secondary hypertension
  • History of respiratory disease, heart disease, renal disease, blindness, deafness and cerebrovascular disease.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
30 participants (actual)

Study arms

  • Experimental
    Placebo

    The breathing was performed normally in this groups.

    Other: Placebo

  • Experimental
    Loaded breathing training

    subjects will trained to inspire deeply against the resistance setting by using BreathMAX® at the loaded of 18 cmH2O with breathing frequency control at 6 breaths/minute. Breathing pattern will be controlled at duty cycle of 0.4 (inspiratory time = 4 sec and total respiratory time = 10 sec). The training program will be performed at home for 30 minutes/day, 7 days/week for 8 weeks.

    Other: Loaded breathing training

  • Experimental
    Unloaded breathing training

    subjects will trained to inspire deeply (no resistance) with breathing frequency control at 6 breaths/minute. Breathing pattern will be controlled at duty cycle of 0.4 (inspiratory time = 4 sec and total respiratory time = 10 sec). The training program will be performed at home for 30 minutes/day, 7 days/week for 8 weeks.

    Other: Unloaded breathing training

Interventions

  • OtherLoaded breathing training

    7 days/weeks, for 8 weeks

  • OtherUnloaded breathing training

    7 days/week, for 8 weeks

  • OtherPlacebo

    7 days/week, for 8 weeks

06

What researchers measure

Primary outcomes

  1. Resting blood pressure

    Time frame: 4 months

Secondary outcomes

  1. Heart rate

    Time frame: 4 months

  2. Pulse wave velocity

    Time frame: 4 months

  3. Exercise pressure response

    Time frame: 4 months

  4. Heart rate variability

    Time frame: 4 months

  5. cardiac output

    Time frame: 4 months

  6. Flow-mediated dilatation of brachial artery

    Time frame: 4 months

  7. Forearm limb blood flow

    Time frame: 4 months

07

Study locations

1 site
  • Faculty of associated medical science, Khon Kaen University
    Muang, Khon Kaen 40000, Thailand
08

References and documents

Publications

  • Jones CU, Sangthong B, Pachirat O. An inspiratory load enhances the antihypertensive effects of home-based training with slow deep breathing: a randomised trial. J Physiother. 2010;56(3):179-86. doi: 10.1016/s1836-9553(10)70023-0. Erratum In: J Physiother. 2010;56(4):221. PubMed 20795924 ↗

Individual participant data

Plan to share: Undecided

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 12, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02200926
Lead sponsor
Khon Kaen University
Responsible party
Benjarat Sangthong (Cardiopulmonay research, Faculty of associated medical science, Khon Kaen University) — Principal investigator
First posted
Jul 25, 2014
Start date
Jul 2014
Primary completion
Nov 2015
Completion
Sep 2016
Last update
Sep 12, 2016

Study contacts

Benjarat Sangthong, M.Sc.
principal investigator · Faculty of associated medical science, Khon Kaen University, thailand

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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