NCT07373925

Brief Summary

This study will be conducted to investigate the effect of Kinesio taping versus dry cupping therapy in the treatment of thoracic kyphosis

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
48

participants targeted

Target at P25-P50 for not_applicable

Timeline
1mo left

Started Feb 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress80%
Feb 2026Jun 2026

First Submitted

Initial submission to the registry

January 21, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

January 28, 2026

Completed
4 days until next milestone

Study Start

First participant enrolled

February 1, 2026

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2026

Last Updated

January 28, 2026

Status Verified

January 1, 2026

Enrollment Period

4 months

First QC Date

January 21, 2026

Last Update Submit

January 21, 2026

Conditions

Keywords

Kinesio tapingDry Cupping TherapyThoracic Kyphosis

Outcome Measures

Primary Outcomes (1)

  • Pain Intensity Level

    A visual analogue scale (VAS) will be used to measure the intensity of pain. With a score of 0 for no pain and 10 for the worst pain ever, this psychometric response scale, which measures pain intensity based on numerical values, is 10 cm or 100 mm in length. The interclass correlation ranges for the VAS, a validated and dependable measure of pain intensity, are 0.95 to 0.98. Patients rated their level of pain as mild if they scored 3.4 or less, moderate if they scored 3.5 to 7.4, and severe if they scored 7.5 or higher.

    up to 4 weeks

Secondary Outcomes (1)

  • Thoracic-curve angle

    up to 4 weeks

Study Arms (3)

Kinesio taping

EXPERIMENTAL

16 participants will receive Kinesio taping once a week for 4 weeks + traditional treatment

Other: Kinesio tapingOther: Conventional treatment

Dry Cupping Therapy

EXPERIMENTAL

16 participants will receive Dry Cupping Therapy 3 times a week for 4 weeks + traditional treatment

Other: Dry Cupping TherapyOther: Conventional treatment

Conventional treatment

ACTIVE COMPARATOR

16 participants will receive traditional treatment

Other: Conventional treatment

Interventions

Participants in this group will receive three sessions per week for four weeks. Two sessions will include cupping therapy in addition to conventional treatment, while one session will consist of conventional treatment only. Six stationary cups will be placed directly around the thoracic spine three cups on each side of the spine. Reusable acrylic cups of medium diameter (3.5 cm) will be used for each individual at each session. The participant will be asked to lie prone. Before beginning the session, if any signs of dehydration are identified by the therapist, coconut oil will be applied to the region in order to hydrate the skin. cups will initially be applied through two suctions by the hand pump, "moderate" suction, which generates a negative pressure of approximately 300 millibar. For participants who report considerable discomfort, the pressure will slightly be minimized according to the individual sensation. cups will be positioned around the thoracic region for 10 Min.

Dry Cupping Therapy

The subjects in this group will be treated with KT in addition to the traditional treatment for thoracic kyphosis. Elastic tape (Kinesio tape, Kinesio® Tex Classic, Kinesio Holding Corporation, New Mexico, USA) 5 cm in width will be applied on the upper back of participants by a certified physiotherapist. When applying the tape, the participants will be in an upright standing position with both arms along the side of the body in a relaxed position. Taping will be applied from a starting point at the anterior aspect of the acromioclavicular joint and will be applied across the spinous process at T6 with the tape ending around T12 paraspinal muscle. The elastic tape will be applied with a stretch of approximately 150 %, .Taping will not be taken off for four days. After day four, it will be taken off and the skin will be rested for two days. Taping application will be repeated on day 7. The patients in this group will be followed for four weeks.

Kinesio taping

The participants in this group will receive conventional treatment that will include advices, stretching, strengthening and functional exercises 3 sessions a week for 4 weeks.

Conventional treatmentDry Cupping TherapyKinesio taping

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Subjects with thoracic kyphosis angle \> 40° diagnosed by a medical doctor will be selected from Damietta University's clinic of physical education faculty.
  • Subjects from both genders with an age range between 18 and 30 years .
  • Subjects who are physically active in physical education sessions

You may not qualify if:

  • Subjects with medical conditions that restrict activity.
  • Those who received exercise intervention for kyphosis.
  • Structural thoracic kyphosis, defined as thoracic kyphosis that did not partially or completely disappear during prone extension, as assessed by a physical therapist.
  • Medical history of spinal fracture, spinal surgery, shoulder joint injury or pelvic injury.
  • Other spinal diseases; presence of scoliosis on Adam's forward bend test.
  • Spinal kyphosis due to visible thoracic deformity.
  • Subjects undergoing professional sports training.
  • Skin disease (dermatitis, psoriasis), neurological disease or cancer.
  • Using anticoagulants or nonsteroidal antidepressants.
  • Inflammatory or rheumatologic disorders of the spine.
  • Severe cardiopulmonary disease, rheumatic disease or pregnancy.
  • Have a pacemaker or metal implants.
  • Do not understand the written consent form.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

Aya Sultan, Master

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
sealed envelopes
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Kinesio taping and Dry Cupping Therapy
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal investigator: Aya Alaa Eldeen Sultan

Study Record Dates

First Submitted

January 21, 2026

First Posted

January 28, 2026

Study Start

February 1, 2026

Primary Completion (Estimated)

June 1, 2026

Study Completion (Estimated)

June 1, 2026

Last Updated

January 28, 2026

Record last verified: 2026-01