Effect of Breathing and Muscle Relaxation Technique in Individual With Essential Hypertension

Sponsor
King Saud University (Other)
Overall Status
Completed
CT.gov ID
NCT05684666
Collaborator
(none)
64
1
4
8.1
7.9

Study Details

Study Description

Brief Summary

Primary hypertension, also called essential hypertension, is a rise in blood pressure (BP) with no identifiable cause. The most prevalent form of hypertension is essential hypertension, which involves 95% of patients with hypertension.Progressive muscle relaxation (PMR) is learning to relax some groups of muscles while paying attention to the feelings connected with both the tense and relaxed states.It is generally established that regular slow (deep) breathing exercises enhance respiratory and cardiovascular function by enhancing parasympathetic tone and reducing sympathetic activity, thus reducing BP, heart rate, respiratory rate, and stress levels in hypertensive patients. This study aimed to investigate the combined effect of slow breathing and PMR technique on BP, heart rate, respiratory rate, and anxiety in patients diagnosed with essential hypertension.

Condition or Disease Intervention/Treatment Phase
  • Other: Slow Breathing Exercise (SBE)
  • Other: Progressive Muscle Relaxation (PMR) Technique
N/A

Detailed Description

From the previously published literature, it is obvious that both slow breathing and PMR and slow breathing is effective in patients with essential hypertension. However, no studies are available on the combined effect of these two techniques. So, the study aims to investigate the combined effect of slow breathing and PMR technique on BP, heart rate, respiratory rate, and anxiety in patients diagnosed with essential hypertension.

Sixty-four participants diagnosed with essential hypertension were randomly allocated into four groups (Slow breathing (SB), PMR, SB+PMR, Control) with 16 subjects in each. Baseline BP, HR, RR and perceived stress scale were taken. All three-intervention groups underwent 30 minutes of training three days before the day of the intervention. The intervention consisted of 30 minutes, pre, mid and post-intervention BP, HR, RR and Perceived Stress (PS) were measured. The control group rested for 30 minutes. Pre, mid and post-rest measurements of BP, HR, RR and PS were taken.

Study Design

Study Type:
Interventional
Actual Enrollment :
64 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Effect of Slow Breathing and Progressive Muscle Relaxation Technique in Individual With Essential Hypertension: a Randomized Controlled Trial
Actual Study Start Date :
Jan 21, 2019
Actual Primary Completion Date :
Aug 30, 2019
Actual Study Completion Date :
Sep 26, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: SBE Group

Slow Breathing Exercise (SBE) was performed by the participants of SBE group. Sixteen participants included in this group.

Other: Slow Breathing Exercise (SBE)
Slow Breathing Exercise (SBE) delivered in a relaxed supine posture on a couch with keeping the feel flat and knee flexed to 90 degree. Participants were instructed to make six breaths per minute for 30 minutes per session, twice a week for 4 weeks.

Experimental: PMR Group

Progressive Muscle Relaxation (PMR) Technique was performed by the participants of the PMR group. It included 16-participants for the study.

Other: Progressive Muscle Relaxation (PMR) Technique
Progressive Muscle Relaxation (PMR) Technique delivered in a relaxed supine posture on a couch with keeping the feel flat and knee flexed to 90 degree. Participants were instructed to complete all sixteen steps of PMR technique for 30 minutes per session, twice a week for 4 weeks.

Experimental: Combined Group

Sixty participants from the combined group performed both Slow Breathing Exercise and Progressive Muscle Relaxation technique in this study.

Other: Slow Breathing Exercise (SBE)
Slow Breathing Exercise (SBE) delivered in a relaxed supine posture on a couch with keeping the feel flat and knee flexed to 90 degree. Participants were instructed to make six breaths per minute for 30 minutes per session, twice a week for 4 weeks.

Other: Progressive Muscle Relaxation (PMR) Technique
Progressive Muscle Relaxation (PMR) Technique delivered in a relaxed supine posture on a couch with keeping the feel flat and knee flexed to 90 degree. Participants were instructed to complete all sixteen steps of PMR technique for 30 minutes per session, twice a week for 4 weeks.

No Intervention: Control Group

No intervention was received/performed by the sixteen participants of the control group in this study.

Outcome Measures

Primary Outcome Measures

  1. Systolic Blood Pressure (SBP) [8 Weeks]

    SBP was measured using a portable electronic sphygmomanometer.

  2. Diastolic Blood Pressure (DBP) [8 Weeks]

    DBP was measured using a portable electronic sphygmomanometer.

  3. Heart Rate (HR) [8 Weeks]

    Heart Rate was measured using a portable electronic sphygmomanometer.

  4. Respiratory Rate (RR) [8 Weeks]

    RR was measured manually as the number of breaths a participant takes per minute.

  5. Perceived Stress (PS) [8 Weeks]

    Perceived Stress was assessed using the perceived stress scale (PSS) with ten items, each with a five-point Likert scale (where a score of 0 indicates "never," a score of 1 indicates "nearly never," a score of 2 "occasionally," a score of 3 "very often," and a score of 4 "often").

Eligibility Criteria

Criteria

Ages Eligible for Study:
30 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Participants with essential hypertension, a diastolic BP between 90 to 109mm of Hg, a systolic BP of more than 140mm of Hg,

  • Aged between 30 to 60 years, and

  • Self co-operation.

Exclusion Criteria:
  • Participants with secondary hypertension, any physical abnormalities that may disturb the exercise intervention,

  • Participant who cannot perform any relaxation or breathing exercises, and

  • Non-cooperation of participants.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Rehabilitation Research Chair, Department of Rehabilitation Sciences, king Saud University Riyadh Riyadh 11433 Saudi Arabia 10219

Sponsors and Collaborators

  • King Saud University

Investigators

  • Principal Investigator: AMIR IQBAL, MPT, King Saud University, Riyadh 11433, P.BOX 10219, Saudi Arabia

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
AMIR IQBAL, Prinicipal Investigator, King Saud University
ClinicalTrials.gov Identifier:
NCT05684666
Other Study ID Numbers:
  • RRC-2019-04
First Posted:
Jan 13, 2023
Last Update Posted:
Jan 18, 2023
Last Verified:
Jan 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
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 18, 2023