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Diaphragmatic Breathing Exercises and Chronic Non-spesifik Neck and Back Pain

Effects of Diaphragmatic Breathing Exercises Added to Posture and Core Stabilization Training on Pain, Body Awareness and Cardiovascular Parameters in Women With Chronic Non-spesific Neck and Back Pain

Status
Enrolling by invitation
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07683273
Enrollment
42
Registered
2026-07-06
Start date
2026-06-29
Completion date
2027-01-01
Last updated
2026-07-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Back Pain, Neck Pain Musculoskeletal

Keywords

Neck Pain, Back Pain, Breathing Exercises, Work of Breathing

Brief summary

Effects of Diaphragmatic Breathing Exercises Added to Posture and Core Stabilization Training on Pain, Body Awareness and Cardiovascular Parameters in Women with Chronic Non-spesific Neck and Back Pain

Detailed description

This study aimed to investigate additional effect of diaphragmatic breathing exercises on pain, body awareness and cardiovascular parameters in women with chronic non-spesific neck and back pain

Interventions

OTHERDiapragmatic Breathing

In addition to postural and core stabilization exercises, participants in the intervention group will perform diaphragmatic breathing exercises over an 8-week period, with sessions conducted twice weekly. Each session will last approximately 40 minutes.

Participants in the control group will receive a routine exercise program consisting of postural and core stabilization exercises for 8 weeks, performed twice weekly. Each session will last approximately 30 minutes.

Sponsors

Hacettepe University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Having a diagnosis of non-specific chronic neck pain (ICD-10: M54.2) and upper back pain (ICD-10: M54.6) * Having a Visual Analog Scale (VAS) pain score of ≥ 3/10 * Not having received physiotherapy treatment within the previous 3 months * Not being a regular smoker or alcohol user

Exclusion criteria

* Having a history of cervical region surgery * Individuals with diagnostic codes other than M54.2 and M54.6 will be excluded from the study * Having a history of acute infection, major surgical intervention, or malignancy within the past three months * Having neurological, rheumatological, or respiratory system diseases * Being pregnant

Design outcomes

Primary

MeasureTime frameDescription
Pain intensityBaseline and at 8 weeksPain intensity will be assessed using the Visual Analog Scale (VAS). Participants will be asked to mark the point on a 10-cm scale that best represents the intensity of their pain, where 0 indicates "no pain" and 10 indicates "the worst pain imaginable." The distance (in centimeters) from the 0 point to the participant's mark will be measured and recorded as the VAS score.

Secondary

MeasureTime frameDescription
Body awarenessBaselien and at 8 weeksParticipants' body awareness will be assessed using the Body Awareness Questionnaire (BAQ). The Turkish version of the questionnaire was adapted by Karaca (2017), who reported excellent internal consistency (Cronbach's α = 0.91). The BAQ is an 18-item self-report instrument designed to assess individuals' awareness of their own body and internal bodily sensations. Each item is rated on a 7-point Likert scale ranging from 1 ("Never") to 7 ("Always"). Total scores range from 18 to 126, with higher scores indicating greater awareness of bodily signals.
Blood pressureBaseline and at 8 weeksParticipants will be assessed in the seated position after at least 15 minutes of rest. Blood pressure measurements will be obtained twice from the right arm using a manual sphygmomanometer. Systolic and diastolic blood pressure values will be recorded.
Heart rateBaseline and 8 weeksResting heart rate will be measured using a fingertip pulse oximeter

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 7, 2026