Additional identifiers
EudraCT/CTIS number
IRAS number
ClinicalTrials.gov number
Protocol/serial number
N0453192079
Study information
Scientific title
Acronym
Study hypothesis
A sustained natureal apophyseal glide (SNAG) is a technique widely used by physiotherapists to treat patients with neck problems, however, its efficacy in comparison with the standard treatment of exercise is unknown. This study intends to establish which physiotherapy modality is better in improving neck pain. There is a lot of conjectural evidence from the author of the SNAG and case studies. But the technique has not been subjected to the rigorous testing of a randomised clinical trial.
Ethics approval(s)
Not provided at time of registration
Study design
Randomised controlled trial
Primary study design
Interventional
Secondary study design
Randomised controlled trial
Study setting(s)
Hospital
Study type
Treatment
Patient information sheet
Condition
Musculoskeletal Diseases: Neck problems
Intervention
This is to find out if SNAG technique has improved neck exercise. The purpose of the study is to compare two physiotherapeutic techniques to establish which is better in improving pain, stiffness and disability in patients with neck pains. All the patients assessment will take place within the same physiotherapy department by the same physiotherapist. Baseline characteristics of each group will be monitored for age, sex whether the cause of their pain is known or unknown and the length of time of their pain to minimise confounding variables. If a diagnosis of mechanical neck pain is made, and if they meet the inclusion/exclusion criteria they will be asked if they would like to participated in the study. All patients will be given a patient information sheet to take home and read and consult with relatives for a minimum of 48 hours. If they agree to take part in the study they will be asked to sign a consent form. The outcome measures process may take approximately 10 minutes.
Following completion of the 8 week study period if the patients symptoms have not resolved they will receive any other appropriate treatment as necessary with the physiotherapist otherwise they will be discharged.
Intervention type
Other
Primary outcome measure
A change in neck range of motion, measured in degrees and after treatment interventions.
Secondary outcome measures
Not provided at time of registration
Overall study start date
13/02/2007
Overall study end date
13/08/2009
Reason abandoned (if study stopped)
Eligibility
Participant inclusion criteria
Not provided at time of registration
Participant type(s)
Patient
Age group
Not Specified
Sex
Not Specified
Target number of participants
40 in total 20 per group
Participant exclusion criteria
Not provided at time of registration
Recruitment start date
13/02/2007
Recruitment end date
13/08/2009
Locations
Countries of recruitment
England, United Kingdom
Study participating centre
MRI Central Manchester & Manchester Children's University Hospitals
Manchester
M13 9WL
United Kingdom
Sponsor information
Organisation
Record Provided by the NHSTCT Register - 2007 Update - Department of Health
Sponsor details
The Department of Health
Richmond House
79 Whitehall
London
SW1A 2NL
United Kingdom
+44 (0)20 7307 2622
dhmail@doh.gsi.org.uk
Sponsor type
Government
Website
Funders
Funder type
Government
Funder name
Central Manchester and Manchester Children's University Hospitals NHS Trust (UK)
Alternative name(s)
Funding Body Type
Funding Body Subtype
Location
Funder name
NHS R&D Support Funding
Alternative name(s)
Funding Body Type
Funding Body Subtype
Location
Results and Publications
Publication and dissemination plan
Not provided at time of registration
Intention to publish date
Individual participant data (IPD) sharing plan
IPD sharing plan summary
Not provided at time of registration
Study outputs
| Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
|---|