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Completed

NCT Number: NCT05301491

The Effects of Dance Therapy in Women With Chronic Low Back Pain

The aim of this study is to investigate the effect of dance therapy on balance, falling, body awareness and functionality parameters in patients with chronic low back pain. As a result of our study, it is thought that dance therapy will positively affect balance, falling, body awareness and functionality in patients with chronic low back pain compared to conventional therapy.

H 1: Dance therapy improves balance in women with chronic low back pain.

H 2: Dance therapy reduces the risk of falling in women with chronic low back pain.

H 3: Dance therapy increases body awareness in women with chronic low back pain.

H 4: Dance therapy increases functionality in women with chronic low back pain.

H 5: Dance therapy provides more improvement in the parameters investigated compared to conventional therapy in women with chronic low back pain.

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Key information

Age range

18 year–65 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Hasan Kalyoncu University

Gaziantep, Turkey (Türkiye)

About this study

Individuals diagnosed with chronic low back pain and meeting the inclusion criteria are going to be included in the study. These individuals are going to be divided into groups as the odd numbers to study group and even numbers to the control group. Hotpack, ultrasound and Transcutaneous Electrical Nerve Stimulation (TENS) are going to be applied to the patients in the both groups for 3 days a week for 2 months. Besides that, control group is going to perform 40-minute classical exercise program 3 days a week for 2 months. Study group is going to perform dance therapy protocol as indicated below;

  • 10 minutes warm-up (stepping),
  • 25 minutes of dance (such as; steps, figures using hip and knee flexions, hip circulation, and hip rotations)
  • 5 minutes stretching (relaxation) exercises.

Demographic information form is going be filled out patients including information about; age, height (cm), weight (kg), occupation, educational status, bilateral leg length (cm), previous and present diseases, waist/hip ratio, previous surgeries, trunk range of motions, low back pain duration, smoking, falling story. Additionally, following questionnaires are going to be applied to both groups;

  • Short Form Mc Gill Pain Questionnaire,
  • Oswestry Disability Index,
  • Body Awareness Ratio Questionnaire,
  • Nottingham Health Profile Questionnaire,
  • Tampa Kinesiophobia Scale,
  • The World Health Organization Quality of Life (WHOQoL) Scale,
  • Y balance test
  • Time Up and Go (TUG) test

SPSS version 23 (SPSS Inc, Armonk, NY) program will be used in the analysis of the data. Mann Whitney U test, Wilcoxon test and student t test will be analyse methods.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

;

  • Those who agree to participate in the study voluntarily
  • Having low back pain lasting longer than 3 months,
  • Having values between 4 and 7 on the Visual Analog Scale.
  • Female individuals between the ages of 18-65

Exclusion criteria

; Those with a Body Mass Index (BMI) greater than 35 kg/m², pregnant women, those with following problems; neural findings, malignancy, inflammation, arthritis, metabolic bone disease, column vertebralis or lower extremity surgery, cardiovascular system diseases, severe osteoporosis, communication and hearing disorders, and those who illiterate, receive other treatment for low back pain.

Treatment and study plan

Dance Therapy Group

Other

Dance therapy group patients are going to be treated 3 days a week for 8 weeks. Patients who started treatment are going to be randomly divided into groups that includes four individuals, due to COVID-19 pandemic preventions.

Dance therapy is going to be applied with individualized choreographies specially prepared for the patients, taking the expert opinion of the dance therapist. Choreographies of different dance genres (step/aerobic dance, zumba, salsa, bachata, oriental etc.) are going to be used in the program. Sessions are going to be with the practitioner in a bright, clean, empty and noiseless room in front of a full-length wall mirror. The practitioner is going to participate to dance therapy throughout the sessions, allowing patients to imitate movements. Session duration is going to be 40 minutes. Patients will be given a one-minute rest period during music transitions.

Other names: Study Group

Exercise group

Other

The patients in the control group is going to perform conventional low back exercises. The program of the patients will start with stretching and warming exercises, and will continue with strengthening exercises.

Exercises planed for control group;

  • Unilateral hip-knee flexion (self-assisted exercise)
  • Bilateral hip-knee flexion (self-assisted exercise)
  • Straight leg lifting with the aid of a sheet/rigid band
  • Posterior pelvic tilt
  • Bridge building exercise
  • Cat-camel exercise
  • Half shuttle in sagittal plane
  • Right and left rotational shuttle
  • Trunk hyperextension in prone position
  • Rotational exercise with hip-knee flexed in supine position Patients are going to do exercises with ten repetitions. As the sessions progressed, the number of repetitions will be increased.

Other names: Control Group

Pyhsiotherapy Modalities

Other

20 minutes hotpack, 3-5 minutes ultrasound and 20 minutes conventional type Transcutaneous Electrical Nerve Stimulation (TENS) are going to be applied to lumbar region of all patients in prone position.

Other names: Both Groups

Primary outcomes

  1. Change from baseline in Y balance test score

    Time frame: 8 weeks

    Balance score is going to be assess by Y balance test to determine change from baseline.

  2. Change from baseline in Time Up and Go test seconds

    Time frame: 8 weeks

    Falling risk is going to be assess by Time Up and Go test seconds to determine change from baseline.

  3. Change from baseline in body awareness ratio score

    Time frame: 8 weeks

    Body awareness ratio score is going to be assess by Body Awareness Ratio Questionnaire to determine change from baseline.

  4. Change from baseline in functionality score

    Time frame: 8 weeks

    Functionality score is going to be assess by Oswestry Disability Index to determine change from baseline.

Secondary outcomes

  1. Change from baseline in range of motion degree

    Time frame: 8 weeks

    Range of motion degree is going to be assess by goniometric measurement to determine change from baseline.

  2. Change from baseline in waist/hip ratio

    Time frame: 8 weeks

    Waist/hip ratio is going to be assess by measuring tape from waist and hip circumference to determine change from baseline.

  3. Change From Baseline in Pain Scores

    Time frame: 8 weeks

    Pain score is going to be assess by Short Form Mc Gill Pain Questionnaire to determine change from baseline.

  4. Change from baseline in kinesiophobia score

    Time frame: 8 weeks

    Kinesiophobia score is going to be assess by Tampa Kinesiophobia Scale to determine change from baseline.

  5. Change from baseline in quality of life score

    Time frame: 8 weeks

    Quality of life score is going to be assess by WHOQoL Questionnaire to determine change from baseline.

  6. Change from baseline in perceived health status score

    Time frame: 8 weeks

    Perceived health status score is going to be assess by Nottingham Health Profile Questionnaire to determine change from baseline.

Sponsors and collaborators

Lead sponsor

Hasan Kalyoncu University

Other

Registry information

Official study title

Investigation of the Effects of Dance Therapy on Balance, Falling, Body Awareness and Functionality in Women With Chronic Low Back Pain

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
Mar 29, 2022
Registry last updated
Aug 11, 2022

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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