Fibromyalgia Clinical Trial
Official title:
The Effect of Pranayama and Diaphragmatic Breathing Exercise on Sleep Quality, Pain and Fatigue Level in Female Patients With Fibromyalgia
NCT number | NCT05840939 |
Other study ID # | 2344633 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | November 11, 2022 |
Est. completion date | June 30, 2023 |
Verified date | January 2024 |
Source | Inonu University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Female patients diagnosed with fibromyalgia were divided into pranayama breathing exercise, diaphragm breathing exercise and control groups. The sleep quality, pain and fatigue levels of the patients in the intervention group were determined before and after the breathing exercise.
Status | Completed |
Enrollment | 100 |
Est. completion date | June 30, 2023 |
Est. primary completion date | December 24, 2022 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: •? Being 18 years or older - Being a female patient who has had pain for at least three months and has been diagnosed with fibromyalgia by a physician according to the ACR 2016 fibromyalgia diagnostic criteria. - Having a PSQI score of five and above - Complaint of fatigue and getting a score of 4 or above on the fatigue severity scale - Pain score of one or above according to VAS - Having no communication problems and knowing how to read, write and speak Turkish - Not being pregnant and not breastfeeding Exclusion Criteria: - Having a malignancy related to the respiratory system (bronchus or lung) - Having tuberculosis disease - Having chest pain - Having any psychiatric diagnosis during outpatient clinic screenings - Having a nasal septum derivation or adenoid that will affect the ventilation process - Having previously practiced/trained in pranayama or diaphragmatic breathing exercises |
Country | Name | City | State |
---|---|---|---|
Turkey | Meltem Sungur | Sahinbey | Gaziantep |
Lead Sponsor | Collaborator |
---|---|
Inonu University | Kilis 7 Aralik University |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Visual Analog Scale (VAS) | "0" indicates no pain and "10" indicates the most severe level of pain. On the scale, <3 mild pain, 3-6 moderate pain, >6 severe pain were specified. | [Time Frame: 6 weeks] |
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