Effects of Diaphragmatic Breathing Exercises on Pain, Grip Strength, and Anthropometric Measures in Women With Chronic Nonspecific Neck Pain
1 other identifier
interventional
40
1 country
1
Brief Summary
Chronic nonspecific neck pain may affect the mechanical loading of the cervical region and trunk stabilization. Diaphragmatic breathing exercises may contribute to postural control and trunk stabilization in addition to their role in breathing. This randomized controlled study investigated the effects of adding diaphragmatic breathing exercises to posture and core stabilization exercises on pain, grip strength, and anthropometric measurements in women with chronic nonspecific neck pain. Forty women aged 18-60 years with chronic nonspecific neck pain lasting at least three months participated in the study. Participants were randomly assigned to an intervention group or a control group, with 20 participants in each group. Both groups performed posture and core stabilization exercises twice weekly for eight weeks. The intervention group additionally performed 10 minutes of diaphragmatic breathing exercises during each session. Pain intensity, right and left hand grip strength, body mass index, waist-to-hip ratio, and waist-to-height ratio were assessed before and after the exercise program. Pain was assessed using the Visual Analog Scale, grip strength using a hydraulic hand dynamometer, and anthropometric measurements according to International Society for the Advancement of Kinanthropometry standards. The results showed that adding diaphragmatic breathing exercises may provide additional benefits, particularly in reducing activity-related pain in women with chronic nonspecific neck pain.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started May 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2026
CompletedFirst Submitted
Initial submission to the registry
September 7, 2026
CompletedFirst Posted
Study publicly available on registry
September 14, 2026
CompletedSeptember 14, 2026
September 1, 2026
4 months
September 7, 2026
September 11, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Resting Pain Intensity
Resting pain intensity was assessed using the Visual Analog Scale (VAS). Participants marked their current pain intensity on a 10-cm line ranging from 0 (no pain) to 10 (worst possible pain). The distance from the starting point was recorded in centimeters.
Baseline and Week 8
Right Hand Grip Strength
Right hand grip strength was measured using a Jamar hydraulic hand dynamometer. Three measurements were performed with a one-minute rest interval between trials, and the highest value was recorded in kilograms
Baseline and Week 8
Secondary Outcomes (2)
Activity Pain Intensity
Baseline and Week 8
Waist-to-Hip Ratio
Baseline and Week 8
Other Outcomes (3)
Left Hand Grip Strength
Baseline and Week 8
Body Mass Index
Baseline and Week 8
Waist-to-Height Ratio
Baseline and Week 8
Study Arms (2)
Diaphragmatic Breathing + Posture and Core Stabilization
EXPERIMENTALParticipants receive posture and core stabilization exercises plus diaphragmatic breathing exercises for 8 weeks, twice weekly.
Posture and Core Stabilization
ACTIVE COMPARATORParticipants receive posture and core stabilization exercises for 8 weeks, twice weekly, without diaphragmatic breathing exercises.
Interventions
Participants perform posture and core stabilization exercises twice weekly for 8 weeks.
Participants in the intervention group perform diaphragmatic breathing exercises for 10 minutes twice weekly for 8 weeks in addition to posture and core stabilization exercises.
Eligibility Criteria
You may qualify if:
- Women aged 18-60 years.
- Presence of non-specific chronic neck pain lasting for at least 3 months.
- No participation in a physiotherapy program during the previous 3 months.
- Voluntary participation in the study and provision of written informed consent.
You may not qualify if:
- Previous cervical spine surgery.
- Acute infection or major surgery within the previous 3 months.
- History of malignancy.
- Neurological, rheumatological, or respiratory disease that could affect study participation or outcomes.
- Pregnancy.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Melike Gültekinlead
Study Sites (1)
Karadeniz Teknik Üniversitesi
Trabzon, Ortahisar, 61080, Turkey (Türkiye)
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- PhD
Study Record Dates
First Submitted
September 7, 2026
First Posted
September 14, 2026
Study Start
May 1, 2026
Primary Completion
September 1, 2026
Study Completion
September 1, 2026
Last Updated
September 14, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will not share
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