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Effectiveness of Massage Therapy With Active Component and Therapeutic Exercise in Cervical Pain

Effectiveness of Massage Therapy With Active Component and Therapeutic Exercise in Cervical Pain

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04856813
Enrollment
42
Registered
2021-04-23
Start date
2021-08-01
Completion date
2022-07-09
Last updated
2022-11-02

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

Conditions

Chronic Pain, Neck Pain

Keywords

neck pain, exercise, Endurance, Training, Intervention

Brief summary

It is an interventional study that proves the eficacy of the manual therapy with active manual therapy and combined with exercise in cervical pain.

Detailed description

The study will be divided in two different groups: * A control group (group A) : they will receive a treatment with manual therapy and physical exercise. * An experimental group (group B) : they will receive the previous treatment, but also the pacient's do active muscle active contraction. The exercise is compound by a home program of several exercises with diferent difficulties. The contraction will consist on a combination of concentric and isometric work. being the patient's pain threshold the one that will guide us to the choice of the predominance of concentric or isometric contraction . Both groups will be joined by a five-minute work on pain education.

Interventions

OTHERManual therapy active

massage or ischemic compression with active contraction, tha will be isometric or concentric.

OTHERManual therapy

massage or isquemic compression without contraction

Sponsors

Alexander Achalandabaso
Lead SponsorOTHER

Study design

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

Intervention model description

blind

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* accept to participate in the study, through informed consent * subjects with chronic nonspecific neck pain lasting equal to or more than 3 months

Exclusion criteria

* Present neck pain caused by serious pathology such as: inflammatory, congenital, infectious, metabolic and neoplastic diseases. * Cervical pathology of traumatic origin with less than 6 months of evolution. * Rheumatic diseases. * Neck pain with neurological signs such as: radiculopathy and myelopathy. * Previous surgery of the cervical spine. * Pregnancy. * Have received physiotherapeutic treatment in the cervical region during the month prior to the inclusion of the study. * Have the intention of receiving other physiotherapeutic treatments different from the one proposed during the study period. * Present serious mental disorders.

Design outcomes

Primary

MeasureTime frameDescription
Change in Neck disabilityBaseline, 1 month (primary timepoint) , 2 months and 5 months after intervention commencement.Using the Neck Disability Index (NDI). It is made up of 10 items and each item is scored on a 6-point Likert scale (0 to 5), leading to a total score ranging from 0 to 50 (0 to 4 = no disability; 5 to 14 = mild disability; 15 to 24 = moderate disability; 25 to 34 = severe disability; and 35 to 50 = complete disability).

Secondary

MeasureTime frameDescription
Change in Range of motion (ROM)Baseline, 1 month (primary timepoint) and 2 months after intervention commencement.Using a inclinometer
Change in craniocervical flexionBaseline, 1 month (primary timepoint) and 2 months after intervention commencement.Using the craniocervical flexion test (CCFT) we make a evaluation of the strength of the deep cervical flexor muscles. From 22 to 30 mmHg of preasure.
Change in pain perceptionBaseline, 1 month (primary timepoint), 2 months and 5 months after intervention commencement.Using the Visual Analog Scale (VAS) from 0 to 10
Change in CatastrophismBaseline, 1 month (primary timepoint), 2 months and 5 months after intervention commencement.Using the Pain catastrophizing scale from 0 to 56
Change in Sleep QualityBaseline, 1 month (primary timepoint) , 2 months and 5 months after intervention commencement.Using the Pittsburgh Sleep Quality Index
Change in kinesophobiaBaseline, 1 month (primary timepoint) , 2 months and 5 months after intervention commencement.Using the Tampa Scale for Kinesiophobia-11 (TSK-11), self-report of 17 items that address fear of movement and injury relapse. Four of the items are negatively written and scored inverse (4, 8, 12 and 16). The scores are added together to obtain a total score, with higher values reflecting greater kinesiophobia.

Countries

Spain

Outcome results

None listed

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