- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05331261
The Effect of Post-Surgery Exercise in Patients With Total Knee Replacement Surgery
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study was designed as a quasi-experimental study to examine the effect of breathing exercise on pain in patients undergoing Total Knee Replacement surgery. This exercise is utterly simple, takes almost no time, requires no equipment and can be done anywhere. Although you can do the exercise in any position, sit with your back straight while learning the exercise. Place the tip of your tongue against the ridge of tissue just behind your upper front teeth, and keep it there through the entire exercise. You will be exhaling through your mouth around your tongue; try pursing your lips slightly if this seems awkward.
- Exhale completely through your mouth, making a whoosh sound.
- Close your mouth and inhale quietly through your nose to a mental count of four.
- Hold your breath for a count of seven.
- Exhale completely through your mouth, making a whoosh sound to a count of eight.
- This is one breath. Now inhale again and repeat the cycle three more times for a total of four breaths.
This study was designed as a quasi-experimental study to examine the effect of breathing exercise on pain in patients undergoing Total Knee Replacement surgery. Note that you always inhale quietly through your nose and exhale audibly through your mouth. The tip of your tongue stays in position the whole time. Exhalation takes twice as long as inhalation. The absolute time you spend on each phase is not important; the ratio of 4:7:8 is important. If you have trouble holding your breath, speed the exercise up but keep to the ratio of 4:7:8 for the three phases. With practice you can slow it all down and get used to inhaling and exhaling more and more deeply.
This exercise is a natural tranquilizer for the nervous system. Unlike tranquilizing drugs, which are often effective when you first take them but then lose their power over time, this exercise is subtle when you first try it but gains in power with repetition and practice. Do it at least twice a day. You cannot do it too frequently. Do not do more than four breaths at one time for the first month of practice. Later, if you wish, you can extend it to eight breaths. If you feel a little lightheaded when you first breathe this way, do not be concerned; it will pass.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Sarıçam
-
Adana, Sarıçam, Turkey
- Çukurova Üniversitesi
-
-
University
-
Adana, University, Turkey
- Çukurova Üniversitesi
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
be over the age of 18,
- Being able to speak Turkish,
- Does not have any barriers in communication, understanding and comprehension,
- Not having visual and hearing impairment,
- Not taking pain medication 60 minutes before or 30 minutes after the intervention,
- Volunteering to participate in the research,
Exclusion Criteria:
-
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: The Effect of 4-7-8 Breathing Technique on Pain
Impact of the 4-7-8 Breathing Technique on Postoperative Pain Following Total Knee Arthroplasty
|
Breath exercises
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
NRS Scale
Time Frame: Bir dakika
|
NRS is a unidimensional scale that uses 11 numbers (from 0 to 10) to measure pain intensity.32
The patient is asked to choose the number that best reflects their pain intensity (0=no pain at all, 10= the worst pain).
|
Bir dakika
|
Collaborators and Investigators
Sponsor
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 (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ARKeskin
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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