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Dry Needling and cupping therapy in Hamstring muscle

Comparison of the Effects of Dry Needling and Cupping therapy on Pain Intensity, Range of Motion, and Function of the Hamstring Muscle with Active Myofascial Trigger Points in amateur athletes

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20260214068853N1
Enrollment
30
Registered
2026-04-20
Start date
2026-04-20
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Hamstring Muscle with Active Myofascial Trigger Points.

Interventions

Intervention group:.

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Patients with active trigger points in the hamstring muscle (assessed by physiotherapist) Pain intensity according to the VAS scale between 3 and 7 Amateur athletes (3 sessions per week or maximum 6 hours of weekly training for at least the last 10 months) Individuals with hamstring muscle shortening with AKE 90/90 (physiotherapist assessment)

Exclusion criteria

Exclusion criteria: Having a history of orthopedic or neurological problems in the lower extremities Having a history of surgery in the back, hip, or knee areas Having a recent history of hamstring strain Having upper or lower motor neuron damage Received treatment in the last three months women in menstruation cycle Having a difference in limb length of more than two centimeters Experience of any injury to the lower extremities within the last three months

Design outcomes

Primary

MeasureTime frame
Hamstring flexibility with active knee extension test, pain intensity with VAS or visual analogue scale, passive compliance of hamstring , peak passive torque during stretch. Timepoint: The assessment periods include one session before the start of treatment, one immediately after the first session, a third after the completion of treatment sessions, and a fourth two weeks after the assessments for follow-up. Method of measurement: Visual Analog Scale (VAS) for pain, Goniometer, Handheld dynamometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSara Delsuz

Tehran University of Medical Sciences

saraslifeonig@gmail.com+98 21 5635 0670

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026