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N/A N=43 Randomized Single-blind Treatment

Benefit of Adding Stretching to Standard Intervention For Patients With Nonspecific Mechanical Neck Pain

Neck Pain

Enrolled (actual)
43
Serious AEs
0.0%
Results posted
Oct 2019
Primary outcome: Primary: Cervical Range of Motion — 46.2; 46.1; 71.2; 68.5 Degree

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
combined intervention group (Other); The standard intervention (Other)
Age
Adult · 18+ yrs
Sex
All
Sponsor
Loma Linda University
Primary completion
Jan 2018

Outcome Measures

OutcomeResultp-value
PRIMARY
Cervical Range of Motion
53.9; 53.2; 79.2; 74.5; 78.5; 71.5
PRIMARY
Cervical Range of Motion
53.9; 53.2; 79.2; 74.5; 78.5; 71.5
PRIMARY
Cervical Range of Motion
53.9; 53.2; 79.2; 74.5; 78.5; 71.5
PRIMARY
Cervical Range of Motion
53.9; 53.2; 79.2; 74.5; 78.5; 71.5
SECONDARY
Numeric Pain Rating Scale
1.5; 1.8
SECONDARY
Numeric Pain Rating Scale
1.5; 1.8
SECONDARY
Numeric Pain Rating Scale
1.5; 1.8
SECONDARY
Numeric Pain Rating Scale
1.5; 1.8
SECONDARY
Neck Disability Index
3.7; 6.5
SECONDARY
Neck Disability Index
3.7; 6.5
SECONDARY
Neck Disability Index
3.7; 6.5
SECONDARY
Neck Disability Index
3.7; 6.5
SECONDARY
Global Rating of Change
4.9; 3.3
SECONDARY
Global Rating of Change
4.9; 3.3
SECONDARY
Global Rating of Change
4.9; 3.3
SECONDARY
Pressure Pain Threshold
5.8; 4.9; 5.5; 5.4
SECONDARY
Pressure Pain Threshold
5.8; 4.9; 5.5; 5.4
SECONDARY
Pressure Pain Threshold
5.8; 4.9; 5.5; 5.4
SECONDARY
Pressure Pain Threshold
5.8; 4.9; 5.5; 5.4

Summary

The purpose of this study is to assess the benefit of adding stretching exercises to cervical mobilization and cervical range of motion exercises on cervical range of motion, pain, pain threshold, level of disability and patient satisfaction for patient with non-specific mechanical neck pain

Eligibility Criteria

Inclusion Criteria

  • The participant will be eligible to participate in the study if he or she is between 18 and 60 years of age, had non-specific neck pain for at least 2 weeks

Exclusion Criteria

  • Participants will be excluded from the study if they had one or more of the following conditions: had previous surgery in cervical spine area, chronic disease such as diabetes, vertigo, dizziness, fracture of the cervical vertebra or scapula, multiple sclerosis, osteoporosis, rheumatoid arthritis or osteoarthritis as approximately 60% of people who aged between 50-60 years will have osteoarthritis.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03194490). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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