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Bowen therapy and tennis ball technique in patients with thoracic myofascial pain syndrome

Comparative effects of Bowen therapy and tennis ball technique on pain and functional disability in patients with thoracic myofascial pain syndrome

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190717044238N7
Enrollment
30
Registered
2023-03-19
Start date
2023-03-06
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Thoracic myofascial pain syndrome. Unspecified soft tissue disorder related to use, overuse and pressure

Interventions

Intervention 1: Intervention group: group A will receive Bowen therapy, the position of ease will be produced and then small moves at varying pressure will be applied.The treatment will include light

Sponsors

Ripah international university Lahore
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Both male and female patients Age group 18-40 years Only patients reporting pain on numeric pain rating scale above 4 Individuals fulfilling the criteria of five major(spontaneous pain, palpable taut band, localized sharp tenderness, referred pain, decreased ROM) and at least one out of three minor signs (pain on pressure, local twitch response (LTR), decrease in pain by muscle stretching) of myofascial pain syndrome will be included.

Exclusion criteria

Exclusion criteria: Patients with fibromyalgia Individuals with any other deformity like scoliosis. Participant taking anti-inflammatory drugs will be excluded

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Total intervention protocol will be given for four weeks of duration, 3 sessions per week with total 12 sessions. Outcomes wiil be assessed at baseline, at the end of 2nd week (6th session) and at the end of the 4th week (12th session). Method of measurement: Numeric Pain Rating Scale (NPRS).

Secondary

MeasureTime frame
Functional Disability. Timepoint: Total intervention protocol will be given for four weeks of duration, 3 sessions per week with total 12 sessions. Outcomes wiil be assessed at baseline, at the end of 2nd week (6th session) and at the end of the 4th week (12th session). Method of measurement: Pain Disability Questionnaire.

Countries

Pakistan

Contacts

Public ContactAfsheen Khalid

Riphah International University Lahore

afsheenkhalid11@gmail.com+92 324 4558262

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 9, 2026