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Active Intervention for Patients With Neck Pain

Effects of an Active Program in Patients With Chronic Neck Pain: a Randomized Controlled Trial.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03987516
Enrollment
50
Registered
2019-06-17
Start date
2019-06-11
Completion date
2019-09-11
Last updated
2019-09-04

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

Conditions

Neck Pain

Brief summary

Neck pain is a complex biopsychosocial disorder often precipitated or aggravated by neck movements or sustained neck postures. More than 80 % of individuals experience neck pain and neck associated disorders. The aim of this study was to investigate the effects of a 4-week active exercising program in patients with chronic neck pain.

Detailed description

While neck pain can be severely disabling and costly, treatment options have shown moderate evidence of effectiveness. The optimal physiotherapy intervention is currently unclear. Consequently, more research in this area combining different techniques in patients with a specific clinical profile is needed. It has been previously shown that participants prefer self-care measures for the management of neck pain. The aim of this study was to investigate the effects of a 4-week active exercising program in patients with chronic neck pain.

Interventions

OTHERActive exercising

Patients allocated to the experimental group were included in an active exercising program adapted to each patient

Sponsors

Universidad de Granada
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* To suffer from chronic neck pain (at least 3 months' duration) * Neck pain of at least 3 on a visual analogue scale. * Participants' symptoms should be at least partly related to increased nerve mechanosensitivity in the neck and upper limb confirmed by the reproduction of participants' symptoms by median nerve upper-limb neurodynamic test.

Exclusion criteria

* Whiplash related neck pain. * Previous cervical surgical intervention. * Cognitive impairments which prevent them to follow instructions. * Visual or acoustic limitations.

Design outcomes

Primary

MeasureTime frameDescription
Changes in number of active trigger pointsChanges from baseline to 4 weeks in the number of active trigger points assessed by palpation. The percentage of active trigger points is obtained.Baseline, 4 weeks

Secondary

MeasureTime frameDescription
Severity of painChanges from baseline to 4 weeks in the severity of pain assessed using the Brief Pain Inventory. The severity and the interference of pain with daily life subscales were included. Score is the sum of the items divided by the number of items.Baseline, 4 weeks
FunctionalityChanges from baseline to 4 weeks on functionality assessed using the Neck Outcome Score.Symptoms, sleep disturbance, every day activity and pain and participation in everyday life subscales were included. They Ranged from 0 to 100 (no simptoms).Baseline, 4 weeks

Countries

Spain

Contacts

Primary ContactMarie Carmen Valenza, PhD
cvalenza@ugr.es958248035

Outcome results

None listed

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