- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05650138
Effects of Jacobson's Progressive Muscular Relaxation Technique in Hypertensive Patients
Effects of Jacobson's Progressive Muscular Relaxation Technique on Blood Pressure Regulation and Activity of Daily Living in Hypertensive Patients
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Hypertension is a disease that becomes a major problem of health. In 2008, 40% of adults aged 25 years above were diagnosed with hypertension. The mortality rate of the complications of hypertension reaches 9.4 million deaths worldwide each year. Hypertension is often called a ''silent killer'' because it often appears without symptoms until it becomes severe and impacts on other organs. Hypertension affects both on physical and psychological. Several studies have found that hypertension can cause anxiety. Hypertension requires comprehensive pharmacological and non-pharmacological treatment. Since 1983, the World Health Organization has suggested the use of the non-pharmacological approach in hypertension treatment. Progressive Muscle Relaxation (PMR) is one of the therapies that is mostly used in complementary therapy and alternative medication. PMR is a technique developed by Edmund Jacobson in 1920. This technique is designed to create a state of physiological and psychological relaxation in patients. It requires the patient to tense and relax various muscle groups while focusing awareness on proprioceptive and interceptive sensations. Several studies have found that PMR exercise helps to reduce blood pressure. Besides, PMR exercise can also reduce anxiety in various diseases.
Study design will be randomized controlled trial. Study will be conducted at Life care Hospital Gujranwala. Written informed consent will be obtained. Patients will be allocated randomly. Subjects meeting the predetermined inclusion and exclusion criteria . Questionnaire will be used as subjective measurements of activity of daily living and Bp will be monitored for initial readings.subjects will be divided into two groups both groups will perform 30 minutes walk as baseline treatment. only one group will receive Jacobsons muscle relaxation technique. Patients will be demonstrated with the technique to contract and relax various groups of muscles, to coordinate contractions and relaxations with deep breaths and to perform the entire procedure with eyes closed in supine lying down position. Every subject will perform this supervised relaxation for 6 repetitions during a single session on once a day basis for four weeks. At the end of 4 weeks of treatment session blood pressure will be recorded questionnaire will be filled. The data thus obtained will be considered for statistical analysis
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Punjab
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Gujrānwāla, Punjab, Pakistan, 50250
- Life care Hospital
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Age: 35 to 55 years
- Ambulatory male and female
- Mentally fitted
- Diagnosed with grade 2 and grade 3 hypertension(3)
Exclusion Criteria:
- Subjects who are not regular in taking medications and who reported about aggravation of any symptoms due to exercise.(7)
- Subjects who fall in grade1 hypertension
- Subjects below the age of 30.
- History of cardiac, renal and liver diseases
- History of recent fracture or surgery.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: jacobson's progressive muscular relaxation technique
Questionnaire will be used as subjective measurements of activity of daily living and Bp will be monitored for initial readings.
They will receive Jacobsons muscle relaxation technique.
Patients will be demonstrated with the technique to contract and relax various groups of muscles, to coordinate contractions and relaxations with deep breaths and to perform the entire procedure with eyes closed in supine lying down position.
Every subject will perform this supervised relaxation for 6 repetitions during a single session on once a day basis twice a week for four weeks.
At the end of 4 weeks of treatment session blood pressure will be recorded questionnaire will be filled
|
subjects will receive Jacobsons muscle relaxation technique.
Patients will be demonstrated with the technique to contract and relax various groups of muscles, to coordinate contractions and relaxations with deep breaths and to perform the entire procedure with eyes closed in supine lying down position.
Every subject will perform this supervised relaxation for 6 repetitions during a single session on once a day basis for four weeks.
30 minutes walk twice a week for 4 weeks
|
|
Active Comparator: 30 min walk
4 weeks, twice a week, 30 minutes walk
|
30 minutes walk twice a week for 4 weeks
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
changes in blood pressure
Time Frame: twice a week for four weeks
|
subjects will receive Jacobsons muscle relaxation technique.
Patients will be demonstrated with the technique to contract and relax various groups of muscles, to coordinate contractions and relaxations with deep breaths and to perform the entire procedure with eyes closed in supine lying down position.
Every subject will perform this supervised relaxation for 6 repetitions during a single session on once a day basis for four weeks.
|
twice a week for four weeks
|
|
Barthel Index for Activity of daily living
Time Frame: four weeks
|
The Barthel Index (BI) measures the extent to which somebody can function independently and has mobility in their activities of daily living feeding, bathing, grooming, dressing, bowel control, bladder control, toileting, chair transfer, ambulation and stair climbing.
|
four weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Sumera abdulhameed, ms, Riphah International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/RCR&AHS/22/0338
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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