The Effectiveness of Patient-tailored Treatment in Patients With (Sub)Acute Neck Pain
Neck Pain, Acute Pain, Rehabilitation
About this trial
This is an interventional treatment trial for Neck Pain focused on measuring stratified care, patient-tailored therapy, subacute
Eligibility Criteria
Inclusion Criteria:
- Non-specific neck pain, pain located in the cervico-thoracic and posterior shoulder region; without dominant arm pain.
- NDI scores score ≥10 % (more than no disability) and ≤68 % (less than complete disability)
- (Sub)acute complaints: <3 months
- Recurrent complaints but no neck pain episode the previous 3 months.
- Mean pain intensity scores: NRS > 3/10
Exclusion Criteria:
- Structural pathology, confirmed by imaging (disk herniation, nerve root compression, radiculopathy, severe rheumatoid diseases, fractures, traumatic alterations…) Shoulder pathology, vestibular pathology.
- Risk stratification: Startback tool for neck pain: high risk group
- BMI > 30 kg/m²
- Other cardiovascular/metabolic/systemic/ neurological diseases, fibromyalgia or chronic fatigue syndrome
- Psychiatric illnesses, history of depression, serious catastrophizing thoughts and/or low treatment expectations.[52]
- Chronic complaints (>3 months) or traumatic onset of the complaints
- Probable or definite neuropathic pain (according to the classification of Finnerup et al.)
- History of surgery in the head/neck or shoulder region
- Hypermobile patients
- Pregnancy or given birth in the preceding year.
- History of recurrent/chronic low back pain
- Primary headache
Sites / Locations
- Marjolein ChysRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Active Comparator
No Intervention
Patient-tailored treatment group
Non patient-tailored treatment group
Control group
Objectives & approach: The subjects in the PTT group will receive the individual tailored treatment program combining best evidence active and passive treatment strategies (manual therapy, individual exercises) in combination with education tailored to the individual situation of the patient and selected home exercises. 9 individual therapy sessions will be performed, in combination with 9 additional home exercise sessions.. NRS and NDI-scores will be monitored before every treatment. The therapist will register when the cut-off score of 30% NDI reduction is present in order to determine the evolution in pain/disability reduction. The importance of self-efficacy will be emphasized and tailored home-exercises will be monitored and adjusted every week.
Objectives & approach: The NPTT will receive an individual (hands-off) treatment, which includes an active neck exercise program, non-tailored education and non-tailored home exercises, according to a previously published program with good results.53 The sessions will be performed once a week under supervision (9 therapy sessions, standard exercise program) and once a week by the patient at home (9 home exercise sessions, standard exercise program).
The subjects randomized to the control group will not receive any intervention, if necessary medication use is permitted and will be monitored using the iMTAQ. Patients will be asked not to seek other treatment options (if possible). If this is not possible, patients will be considered lost to follow-up.