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Enrolling by invitation NCT07518732

Investigation of the Effect of Thoracic Manipulation and Classical Massage on Pain, Flexibility and Sleep Quality

No phase Interventional MECHANICAL BACK PAIN Sleep Quality

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Classical Massage, Manual therapy.
Who it may be relevant to
Registry conditions: MECHANICAL BACK PAIN, Sleep Quality. Basic parameters: 18 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Investigation Of The Effects Of Thoracic Manipulation And Classical Massage On Pain Flexibility And Sleep Quality In Patients With Mechanical Back Pain

Detailed description

Investigation of the Effect of Thoracic Manipulation and Classical Massage on Pain, Flexibility and Sleep Quality

Interventions

  • Other Classical Massage
    Classical Massage
  • Other Manual therapy
    Manual therapy

Primary outcome measures

  • Pain Assessment [Time frame: From enrollment and after 4 weeks]
  • Sit and Reach test [Time frame: From enrollment and after 4 weeks]
  • Trunk extension [Time frame: From enrollment and after 4 weeks]
  • Lateral flexion [Time frame: from enrollment and after 4 weeks]
Secondary outcome measures (3)
  • endurance test [Time frame: from enrollment and after 4 weeks]
  • Quality of life assessment [Time frame: From enrollment and after 4 weeks]
  • Sleep quality [Time frame: from enrollment and after 4 weeks]

Eligibility criteria

Inclusion criteria

  • Being over 18 and being 65 years old
  • Those who have experienced thoracic back problems for at least 3 years
  • Being able to communicate in Turkish
  • Having reading and writing proficiency
  • To ensure voluntary interest in work
  • Being symptomatic and healthy
  • Those with functional scoliosis

Exclusion criteria

  • Being under 18 or 65 years old
  • Those with congenital and idiopathic scoliosis
  • Cases using cortisone in the last 6 weeks
  • Those who do not lie face down
  • History of traumatic injury to the Thoracic Spine
  • Those who have had spinal surgery
  • Those diagnosed with osteoporosis, bone tumor and rheumatoid
  • Pregnancy
  • Individuals with a history of neurological diseases (stroke, multiple sclerosis, Parkinson's)
  • History of cancer

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Turkey (Türkiye) · 1 center
  • Bigadic Saglikli Yasam Merkezi — Istanbul

Identifiers

NCT: NCT07518732 · İRU-FTR-AB-01 · Istanbul Rumeli University

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗