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Effectiveness between single bout- and one week-spot marching programme in chronic non-specific neck pain with central sensitisation

Effectiveness between single bout- and one week-spot marching programme in chronic non-specific neck pain with central sensitisation

Status
Unknown
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20240929004
Enrollment
74
Registered
2024-09-29
Start date
2024-09-02
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

chronic non-specific neck pain with central sensitisation chronic neck pain central sensitisation

Interventions

Spot marching exercise with shoulders flexion at least 90 degrees and hip and knee flexion at least 60 degrees for 30 mins. The exercise intensity will be submaximal (70-85 percent of maximal heart r
Experimental Other,Active Comparator Other
Single bout-spot marching programme,One week-spot marching programme

Sponsors

Naresuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Participants aged 18-65 years presenting with non-specific neck pain at least 12 weeks and central sensitisation inventory atl east 40 scores.

Exclusion criteria

Exclusion criteria: 1 Diagnosed to cervical spondylosis, disc herniation and cervical instability 2 Severe pathologies or red flags such as infection, fracture, cancer, severe osteoarthritis, rheumatoid arthritis, and osteoporesis 3 History of surgery within 1 year 4 Medication use such as pain killers, relaxants and NSAID within 2 weeks 5 Massage and acupuncture within 2 weeks 6 Physiotherapy for cervical treatment within 6 months 7 Skin infection 8 Cervical radiculopathy 9. Open wound 10. Traumatic neck pain 11. Numerical pain rating scale less than 3/10 12. Asthma 13. Anemia 14. HIV 15. Diabetes 16. Aerobic exercise at least 3 times a week within 4 week

Design outcomes

Primary

MeasureTime frame
Numerical rating scale for pain intensity At baseline and 1-week follow-up for both arms Questionnaire,Central sensitisation inventory At baseline and 1-week follow-up for both arms Questionnaire,Neck disability index At baseline and 1-week follow-up for both arms Questionnaire,Fear-avoidance beliefs questionnaire At baseline and 1-week follow-up for both arms Questionnaire,Pain catastrophizing scale At baseline and 1-week follow-up for both arms Questionnaire,SF-36 At baseline and 1-week follow-up for both arms Questionnaire,Pressure pain threshold At baseline and 1-week follow-up for both arms Digital pressure algometer,Blood lactate concentration Before, after exercise, and 30 mins following exercise for arm 1 Taking blood sample,Pressure pain threshold Before, after exercise, and 30 mins following exercise for arm 1 Digital pressure algometer,Numerical rating scale for pain intensity Before, after exercise, and 30 mins following exercise for arm 1 Questionnaire

Secondary

MeasureTime frame
N/A N/A N/A

Countries

Thailand

Contacts

Public ContactTaweewat Wiangkham

Naresuan university

taweewatw@nu.ac.th0908918669

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026