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

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

Status
Enrolling by invitation
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07518732
Enrollment
60
Registered
2026-04-09
Start date
2026-04-01
Completion date
2026-05-10
Last updated
2026-04-09

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

Conditions

MECHANICAL BACK PAIN, Sleep Quality

Keywords

Mechanical Back Pain, Massage, Manipulation, Flexibility, Sleep Quality, Pain

Brief summary

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

Classical Massage

OTHERManual therapy

Manual therapy

Sponsors

Ayşe BAŞAYAN
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Pain AssessmentFrom enrollment and after 4 weeksVAS will be used to measure pain intensity. A 10 cm long line is used, where 0 represented no pain and 10 represented very severe pain. The distance from the marked point to 0 is recorded as a VAS score.
Sit and Reach testFrom enrollment and after 4 weeksThe participant is asked to sit with their feet extended under the test bench. Without bending their knees, they are asked to lean their body forward and reach as far as possible on their fingertips, holding at that point for 2 seconds.
Trunk extensionFrom enrollment and after 4 weeksTrunk extension: In the trunk extension flexibility test, the participant stands facing the wall, with their hips and torso in contact with the wall. The distance between the sternal notch and the wall is measured using a tape measure.
Lateral flexionfrom enrollment and after 4 weeksRight and left trunk lateral flexion flexibility test: The participant is positioned standing; feet shoulder-width apart, knees straight, torso upright, hips and shoulders in a neutral position. The participant's middle finger is used as the measurement point. During the measurement, the zero point of the measuring tape is placed in line with the middle finger.

Secondary

MeasureTime frameDescription
endurance testfrom enrollment and after 4 weeksThe dynamic sit-up test is used to assess the endurance of the trunk flexor muscles of the participants, and the trunk extensor muscle endurance test is used to assess trunk extensor muscle endurance. In these measurements, the number of repetitions completed by the participants in 60 seconds is noted.
Quality of life assessmentFrom enrollment and after 4 weeksThe Short Form-36 will assess mental and physical health. This form will examine participants' physical and mental health status across eight sub-dimensions. Quality of life will be assessed through eight sub-dimensions: physical function, social function, physical role difficulty, emotional role difficulty, mental health, vitality, body pain, and general health.
Sleep qualityfrom enrollment and after 4 weeksThe Pittsburgh Sleep Quality Index (PSQI) will be used as a valid and reliable assessment tool to provide information about participants' sleep quality, as well as the type and severity of sleep disturbances over the past month. The scale will consist of 19 self-reported items and 7 sub-dimensions. In this measure, the following parameters will be evaluated: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleep medication, and daytime dysfunction. Each item on the scale will be scored between 0 and 3.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 10, 2026