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Stabilization Exercises With and Without Connective Tissue Massage for Chronic Mechanical Neck Pain

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02424032
Enrollment
53
Registered
2015-04-22
Start date
2013-02-28
Completion date
Unknown
Last updated
2015-04-22

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

Conditions

Neck Pain Musculoskeletal

Keywords

Neck pain, stabilization exercise, connective tissue massage

Brief summary

The aim of this study was to investigate and compared the effects of cervical and scapulothoracic stabilization exercises with and without connective tissue massage (CTM) for patients with chronic mechanical neck pain.

Detailed description

Sixty patients with chronic mechanical neck pain were recruited and randomly allocated into stabilization exercise with and without the connective tissue massage program. The study's inclusion criteria were as follows: 18 to 65 years of age, having neck pain for more than 3 months, and being volunteer. The exclusion criteria were as follows: stenosis, traumatic injury history, previous surgery related to cervical spine, hypermobility, cancer, having inflammatory rheumatologic, severe psychological disorders, being pregnant, and intervention including exercise or physical therapy in the last 3 months.The program was carried out for 12 sessions, 3 days/week in 4 weeks. Pain intensity with Visual Analog Scale, pressure pain threshold with digital algometer, the level of anxiety with the Spielberger State Trait Anxiety Inventory, and life quality with Short Form-36 were evaluated before and after treatment.

Interventions

BEHAVIORALExercise and connective tissue massage

Cervical and scapulothoracic stabilization exercises with connective tissue massage were performed.The program was carried out for 12 sessions, 3 days/week in 4 weeks.

BEHAVIORALExercise

Cervical and scapulothoracic stabilization exercises were performed. The program was carried out for 12 sessions, 3 days/week in 4 weeks.

Sponsors

Seyda TOPRAK CELENAY
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* 18 to 65 years of age, * having neck pain for more than 3 months, and * being volunteer

Exclusion criteria

* Stenosis, * traumatic injury history, * previous surgery related to cervical spine, * hypermobility, * cancer, * having inflammatory rheumatologic, * severe psychological disorders, * being pregnant, and * intervention including exercise or physical therapy in the last 3 months

Design outcomes

Primary

MeasureTime frame
Change in Neck pain intensity as measured by Visual Analog ScaleChange from baseline neck pain intensity at 4 weeks

Secondary

MeasureTime frame
Change in level of anxiety as assessed by Spielberger State Trait Anxiety InventoryChange from baseline level of anxiety at 4 weeks
Change in quality of life as assessed by Short Form-36Change from baseline quality of life at 4 weeks
Change in pressure pain threshold as measured by digital algometerChange from baseline pressure pain threshold at 4 weeks

Countries

Turkey (Türkiye)

Contacts

Primary ContactSeyda TOPRAK CELENAY
sydtoprak@hotmail.com+90-534-041-3986
Backup ContactDerya OZER KAYA
deryaozer2000@yahoo.com+90-232-329-3513

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026