ClinicalTrials.gg
Not yet recruitingNCT07917702Updated Nov 4, 2026

Effects of Transcranial Direct Current Stimulation and Manual Therapy on Musculoskeletal Pain in Adolescent Dancers

An interventional study of Active Transcranial Direct Current Stimulation and Sham Transcranial Direct Current Stimulation in Musculoskeletal Pain, Chronic Pain and Kinesiophobia, sponsored by Gwangju Health University. Not yet recruiting at 1 site in South Korea. Open to participants aged 13 Years to 18 Years. Per ClinicalTrials.gov, last updated 2026-11-04.

Sponsored by Gwangju Health University · Not applicable, Interventional, and Treatment

Updated Nov 4, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
24
Allocation
Randomized
Ages
13 Years to 18 Years
Sex
All
01

Study summary

Adolescent dancers are at high risk of musculoskeletal pain due to repetitive, high-intensity training. Persistent pain may lead to kinesiophobia (fear of movement), which can further impair physical function according to the fear-avoidance model. Transcranial direct current stimulation (tDCS) has been used as a top-down intervention for musculoskeletal pain; however, it remains unclear whether its analgesic effect results from true neural stimulation or from contextual factors such as treatment expectation.

This three-arm, single-blind randomized controlled trial will enroll 24 adolescent dancers aged 13 to 18 years with musculoskeletal pain lasting at least 3 months. Participants will be randomly allocated, stratified by pain site, to (1) active tDCS plus manual therapy, (2) sham tDCS plus manual therapy, or (3) sham tDCS plus manual therapy plus structured expectation-enhancement education. Each participant will receive a single intervention session. Outcomes will be assessed before, immediately after, and 1 week after the intervention. The study aims to distinguish the neurophysiological effect of tDCS from the effect of treatment expectation on pain, kinesiophobia, and related outcomes.

02

Conditions studied

  • Musculoskeletal Pain
  • Chronic Pain
  • Kinesiophobia

Keywords

  • Transcranial Direct Current Stimulation
  • Musculoskeletal Manipulations
  • Adolescent
  • Placebo Effect
03

In context

Musculoskeletal Pain

513 studies on the registry are indexed under Musculoskeletal Pain; 113 are open to participants now.

This study's planned enrollment of 24 is below the median of 66 across 360 interventional studies indexed under Musculoskeletal Pain.

Browse Musculoskeletal Pain studies →

Lead sponsor

Gwangju Health University is the lead sponsor of 2 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
13 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adolescent dancers or dance majors aged 13 to 18 years
  • Musculoskeletal pain in a specific body region (e.g., lower back, ankle) for at least 3 months
  • Understanding of the study purpose and voluntary assent from the participant, with written informed consent from a legal guardian

Exclusion criteria

Exclusion Criteria:

  • Metal implants in the head or implanted electronic devices (e.g., cardiac pacemaker)
  • Current pregnancy
  • Current use of psychiatric medication
  • Acute inflammatory disease
  • Bleeding disorder or current use of anticoagulants
  • Recent trauma, surgery, or skin disease at the painful (measurement) site
  • History of epilepsy
  • Any other physical condition that makes participation in the study or intervention inappropriate
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
24 participants (estimated)

Study arms

  • Experimental
    Active tDCS + Manual Therapy (ANT)

    Device: Active Transcranial Direct Current Stimulation · Other: Manual Therapy

  • Sham comparator
    Sham tDCS + Manual Therapy (SCT)

    Device: Sham Transcranial Direct Current Stimulation · Other: Manual Therapy

  • Experimental
    Sham tDCS + Manual Therapy + Expectation-Enhancement Education (ECT)

    Device: Sham Transcranial Direct Current Stimulation · Other: Manual Therapy · Behavioral: Expectation-Enhancement Education

Interventions

  • DeviceActive Transcranial Direct Current Stimulation

    Anodal tDCS delivered at 2 mA for 20 minutes using saline-soaked sponge electrodes, with the anode over the primary motor cortex (C3/C4) and the cathode over the contralateral frontal area according to the international 10-20 system. Current is ramped up and down gradually.

  • DeviceSham Transcranial Direct Current Stimulation

    Identical electrode placement and procedure as active tDCS for 20 minutes, with current delivered only for the first 30 seconds and then turned off.

  • OtherManual Therapy

    Manual therapy including instrument-assisted soft tissue mobilization (Graston technique) applied to the painful region for 15 minutes, with the tool held at 30 to 60 degrees, within a tolerable pain range (VAS 3 to 4).

  • BehavioralExpectation-Enhancement Education

    A 5- to 10-minute structured education session delivered by the investigator using a standardized script that explains the principles and expected effects of the treatment.

06

What researchers measure

Primary outcomes

  1. Change in Pain Intensity (Numeric Pain Rating Scale, NPRS)

    Pain intensity rated on a 0 to 10 scale (0 = no pain, 10 = worst pain imaginable). Higher scores indicate greater pain.

    Time frame: Baseline (before intervention), immediately after intervention, and 1 week after intervention

07

Study locations

1 site
  • Jin's Ballet Academy, Pulse Dance Academy
    Gwangju, South Korea
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Nov 4, 2026
Show all 1 update
  1. Nov 4, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07917702
Lead sponsor
Gwangju Health University
Collaborators
Chonnam National University
Responsible party
Sponsor
First posted
Nov 4, 2026
Start date
Nov 9, 2026 (estimated)
Primary completion
Dec 9, 2026 (estimated)
Completion
Dec 15, 2026 (estimated)
Last update
Nov 4, 2026

Study contacts

Hyunjoong Kim, PhD
Contact
hjkim@ghu.ac.kr
+82-62-958-7598
Hyunjoong Kim, PhD
principal investigator · Gwangju Health University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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