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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04350918
Other study ID # OJO/2020/01
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 23, 2019
Est. completion date January 16, 2020

Study information

Verified date April 2020
Source Obafemi Awolowo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Neck pain is becoming increasingly common throughout the world with a considerable impact on individuals, communities, health-care systems and businesses (Hoy et al, 2011).Neck pain is a common problem within our society affecting individual's physical and social functioning considerably and interfering with the patient's daily activities. There is lack of evidence to allow conclusions to be drawn about the effectiveness of MET when compared with stretching exercises for relieving mechanical neck pain. Therefore, this study is designed to examine the effect of MET, static stretching and to compare their effects on pain intensity and functional disability in patient with mechanical neck pain.


Description:

This experimental study purposively recruited 24 subjects (male: n=10, female: n = 14) with mechanical neck pain from the Outpatient Physiotherapy Department of the Obafemi Awolowo University Teaching Hospitals Complex, Ile-Ife. Subjects were randomly allocated into the MET and SS groups. Subjects in MET group received 6 treatment sessions of Muscle Energy Technique in addition to conventional physiotherapy treatments. Patients in SS group received 6 treatment sessions of Static Stretching in addition to conventional physiotherapy treatments. All subjects were treated twice a week for six weeks. Visual Analogue Scale (VAS) and Neck Disability Index (NDI) were used to assess the pain intensity and functional disability at baseline, 3rd week and 6th week of treatment sessions respectively. Descriptive and Inferential statistics were used to analyse the data. Alpha level was set at < 0.05.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date January 16, 2020
Est. primary completion date December 24, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 40 Years to 65 Years
Eligibility Inclusion Criteria:i. Male and female patients with history of mechanical neck pain of more than 3 months

Exclusion Criteria:

- Patients with acute neck pain

- Subjects were excluded if they have neck pain associated with an underlying pathology such as fracture of the cervical spine, neck pain radiating into the arms or upper extremity or associated with headaches or facial pain, malignancy, infections, inflammatory disorders, osteoporosis or cases of disc prolapse.

- Patients with history of surgery of the cervical spine during the previous 12months

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Muscle Enery Techniques
Group of patients that underwent muscle energy technique as a mean of treatment for the complaint
Static Stretching
Set of patients that had static stretching technique for the treatment for the complaint

Locations

Country Name City State
Nigeria Obafemi Awolowo University Ile Ife Osun

Sponsors (1)

Lead Sponsor Collaborator
Obafemi Awolowo University

Country where clinical trial is conducted

Nigeria, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visual Analogue Scale VAS is a one-dimensional measure of pain intensity, which has been widely used in diverse adult populations, including those with rheumatic diseases (Mc Cormack et al, 1988). pain intensity as none, mild, moderate, or severe, the following cut points on the pain VAS have been recommended: no pain (0-4 mm), mild pain(5-44 mm), moderate pain (45-74 mm), and severe pain (75-100 mm) (Aun et al, 1986) From March 2019 to November 2019, The treatment for each patient was for 6 weeks
Secondary Neck Disability Index (NDI) The NDI can be scored as a raw score or doubled and expressed as a percent (Vernon, 1991). Each session is scored on a 0 to 5 rating scale, in which zero means 'No Pain' and 5 means 'Worst Imaginable Pain'. All the points can be summarized as a total score. The test can be interpreted as a raw score with a maximum score of 50 or as a percentage. From March 2019 to November 2019, The treatment for each patient was for 6 weeks
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