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Enrolling by Invitation

NCT Number: NCT07518732

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

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

Enrolling by Invitation

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Bigadic Saglikli Yasam Merkezi

Istanbul, 10000, Turkey (Türkiye)

About this study

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

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Classical massage

Other

Classical Massage

Manual therapy

Other

Manual therapy

Primary outcomes

  1. Pain Assessment

    Time frame: From enrollment and after 4 weeks

    VAS 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.

  2. Sit and Reach test

    Time frame: From enrollment and after 4 weeks

    The 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.

  3. Trunk extension

    Time frame: From enrollment and after 4 weeks

    Trunk 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.

  4. Lateral flexion

    Time frame: from enrollment and after 4 weeks

    Right 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 outcomes

  1. endurance test

    Time frame: from enrollment and after 4 weeks

    The 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.

  2. Quality of life assessment

    Time frame: From enrollment and after 4 weeks

    The 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.

  3. Sleep quality

    Time frame: from enrollment and after 4 weeks

    The 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.

Sponsors and collaborators

Lead sponsor

Ayşe BAŞAYAN

Other

Registry information

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Apr 9, 2026
Registry last updated
Apr 9, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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