Manual Therapy On Pain, Disability And Quality Of Life
Enrolling by invitationNot applicableNCT07494734
View the official record on ClinicalTrials.gov Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.
This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
The aim of this study is to investigate whether conventional physical therapy combined with manual therapy reduces pain and maintains life support in individuals with chronic mechanical neck pain, compared to conventional physical therapy alone. The study plans to evaluate the combined benefits of both treatment methods and manual therapy. Pain, quality of life, range of motion, and neck injuries will be assessed in the participants. The treatment protocol will be administered twice a week, for a total of 10 sessions over a 5-week period.
Study details
- Official title
- The Effect Of Manual Therapy On Pain, Disability And Quality Of Life In Patients With Chronic Mechanical Neck Pain
- Conditions
- Interventions
- Other: Physical therapy
- Other: Physical therapy and manual therapy
- Sponsor
- Istanbul Rumeli University
- Start date
- 2026-07-23
- Primary completion
- 2026-08-01
- Sex
- All
- Age range
- from 18 Years to 65 Years
- Results posted
- No results posted in this snapshot
- Countries
- Turkey (Türkiye)
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * • Being between 18-65 years of age * Having neck pain that has lasted for at least three months * Having a Visual Analog Scale (VAS) score of at least 3 Exclusion Criteria: * Patients not aged 18-60 years * Pregnant women or those suspected of being pregnant * Individuals with acute inflammatory diseases * Individuals with neurological deficits * Individuals with a positive vertebrobasilar artery test * Individuals with advanced osteoporosis * Individuals who have undergone spinal surgery * Individuals who have received an injection in the cervical region within the last 3 months * Individuals with any neurological or psychiatric disorders
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT07494734