Stabilization Training, Voice And Neck Pain
Effects Of Stabilization Exercises On Head Posture, Vocal Efficiency And Pain In Patients With Nonspecific Chronic Neck Pain
1 other identifier
interventional
38
1 country
2
Brief Summary
This randomized controlled trial investigated the effects of cervical stabilization exercises on head posture, pain, functional status, and voicing efficiency in patients with nonspecific chronic neck pain. Following a six-week exercise program, cervical stabilization exercises resulted in significantly greater improvements in pain intensity, functional disability, craniocervical angle, and maximum phonation time compared with traditional exercises. Both exercise interventions led to significant reductions in pain and improvements in cervical posture; however, no significant changes were observed in acoustic voice parameters. Overall, cervical stabilization exercises demonstrated superior benefits in postural alignment, pain reduction, and functional outcomes.
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 Feb 2022
2 active sites
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
February 1, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 12, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
January 10, 2023
CompletedFirst Submitted
Initial submission to the registry
January 8, 2026
CompletedFirst Posted
Study publicly available on registry
February 10, 2026
CompletedFebruary 10, 2026
February 1, 2026
8 months
January 8, 2026
February 3, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Pain Intensity
Visual Analog Scale (VAS)
10 months
Vocal Efficiency
Maximum Phonation Time (MPT) s/z Ratio
10 months
Secondary Outcomes (2)
Neck Disability
10 months
Acoustic Voice Parameters
10 months
Study Arms (1)
The purpose of this study is to investigate the effects of cervical stabilization exercises applied
EXPERIMENTALThe purpose of this study is to investigate the effects of cervical stabilization exercises applied to patients with nonspecific chronic neck pain, the patients' cervical postural alignment, and changes in neck pain-related clinical parameters on voicing efficiency in patients with nonspecific chronic neck pain (NSCNP).
Interventions
Head posture (craniocervical angle), pain (VAS, NDI) and vocal efficiency (acoustic analysis, maximum phonation time, VHI) were measured at baseline and completion. Participants were assigned to either a stabilization exercise group or a control group receiving conventional exercises. Outcome measures included Demographics and Clinical Characteristics, head and cervical posture, pain and disability indices, and voicing efficiency parameters such as maximum phonation time (MPT) and s/z ratio. Acoustic voice measures and self-reported voice handicap (Voice Handicap Index, VHI) were also assessed.These assessments were performed twice, before and after treatment. Patients with cronic neck pain were randomly divided into two groups: the Cervical Stabilization Exercise Group (n = 20, male:3, female:17) and the Traditional Exercise Group (n = 18, male:4, female:14). The both group received a total of 24 sessions of an exercise program over a six-week period, with five sessions per week for t
Eligibility Criteria
You may qualify if:
- Adults aged 18-60 years, experiencing nonspecific neck pain for at least three months, and reporting a pain score of ≥3 on a 0-10-cm visual analogue scale (VAS) at rest. Participants also had to volunteer to participate.
You may not qualify if:
- Previous musculoskeletal injuries of the neck or shoulder; neurological, orthopedic, oncologic, or congenital musculoskeletal disorders; hearing impairment requiring aids; history of head, neck, or laryngeal surgery; recent upper respiratory infection; laryngeal lesions observed on examination; history of voice therapy; severe respiratory dysfunction in the past five years; physical therapy for neck pain within the last six months; tracheobronchial infection during the study period; and pregnancy.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Suleyman Demirel University Hospital
Isparta, 32260, Turkey (Türkiye)
Suleyman Demirel University
Isparta, 32260, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Ferdi Ferdi Baskurt, professor
Suleyman Demirel University
- PRINCIPAL INVESTIGATOR
Emine Metin, phd
Suleyman Demirel University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Doctor Physical Therapist
Study Record Dates
First Submitted
January 8, 2026
First Posted
February 10, 2026
Study Start
February 1, 2022
Primary Completion
October 12, 2022
Study Completion
January 10, 2023
Last Updated
February 10, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ICF, CSR, ANALYTIC CODE
- Time Frame
- 2 years
- Access Criteria
- sdu
I can share it with other researchers if they want.