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Investigating the effect of dry needling and exercise and posture correction on upper crossed syndrome

Investigating the effect of dry needling and exercise therapy and posture correction on pain and performance and posture of employees with upper crossed syndrome: A clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240708062363N1
Enrollment
26
Registered
2025-07-05
Start date
2024-08-22
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

upper crossed syndrome. Abnormal posture

Interventions

Intervention 1: Intervention group: The intervention consisted of at least 16 20-minute sessions twice a week (8 weeks) of dry acupuncture and home exercise exercises 3 days a week for 8 weeks. These

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Absence of orthopedic disorders and diseases that prevent exercises and are diagnosed by the relevant specialist with examinations and history The patient has not participated in a regular exercise program in the last 4 weeks The patient's willingness to participate in the research project

Exclusion criteria

Exclusion criteria: A history of fractures in the neck and shoulder area History of neck and shoulder surgery Joint diseases Failure to complete the training program based on research objectives

Design outcomes

Primary

MeasureTime frame
Pain intensity based on the NPRS scale. Timepoint: Before and after the intervention. Method of measurement: Questioning the patient.;Photogrammetry. Timepoint: Before and after the intervention. Method of measurement: Determination of neck angle by a doctor.;Visual Analog Scale. Timepoint: Before and after the intervention. Method of measurement: Questioning the patient.;Neck Disability Index. Timepoint: Before and after the intervention. Method of measurement: Questioning the patient.;SF-36 Quality of Life Questionnaire. Timepoint: Before and after the intervention. Method of measurement: Questioning the patient.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactseyed reza hashemi

Tehran University of Medical Sciences

hashemi_3652@yahoo.com+98 21 6658 1637

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026