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The Effectiveness of Cognitive Functional Therapy in Adults With Chronic Neck Pain

E

European University Cyprus

Status

Enrolling

Conditions

Chronic Pain

Treatments

Behavioral: Conventional Therapy
Behavioral: Cognitive Functional Therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT06063408
0101100333

Details and patient eligibility

About

The aim of this study was to compare the effectiveness of Cognitive Functional Therapy compared with Conventional Therapy in treating adults with chronic neck pain

Full description

After being informed about the study and potential risks, all patients giving written informer consent will undergo 1 week screening period to determine eligibility for study entry. At week 0, patients who meet the eligibility criteria will be randomized in a single- blind manner (assessor), in a 1:1 ration to cognitive functional therapy or conventional therapy twice a week for 8 weeks.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 64 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18-64
  • Pain in neck area for more than 3 months
  • Pain in NPRS more than 40/100
  • Independently mobile (with or without aids), to be capable of participating in a rehabilitation program twice a week

Exclusion criteria

  • Serious psychological pathology
  • recently surgery on shoulder or neck area (<6 months)
  • Pain relieving procedures such as injection based therapy (e.g epidurals) and day case procedures (e.g rhizotomy) in the last 3 months
  • Pregnancy
  • Rheumatologic/inflammatory disease (e.g. rheumatoid arthritis (RA), ankylosing spondylitis (AS), psoriatic arthritis, lupus, scheuermann's disease)
  • Progressive neurological disease (e.g. multiple sclerosis (MS), parkinson's disease (PD), motor neuron disease (MND)
  • Unstable cardiac conditions
  • Red flag disorders like malignancy/cancer, acute traumas like fracture (<6 months ago) or infection, spinal cord compression/cauda equina

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

Cognitive Functional Therapy
Experimental group
Description:
Participants will received in this group four main component: 1. Pain education, cognitive education, explanation about their health condition, self management education 2. Graded exposure to painful movements or activities 3. Movement therapy targeted to their functional integration 4. Lifestyle programme.
Treatment:
Behavioral: Cognitive Functional Therapy
Conventional Therapy
Active Comparator group
Description:
Participants will received in this group four main component: 1. Tens therapy 2. Massage to cervical and shoulder area 3. Relaxation techniques 4. Posture exercises 5. Workplace education
Treatment:
Behavioral: Conventional Therapy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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