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IASTM vs. Static Stretching for Hamstring Tightness: Short- and Long-Term Effects (IASTM-HT)

18. september 2026 oppdatert av: GÖKHAN MARAŞ

Comparison of the Short- and Long-Term Effects of Static Stretching and Instrument-Assisted Soft Tissue Mobilization on Flexibility, Performance, and Pressure Pain Threshold in Individuals With Hamstring Tightness: A Randomized Controlled Trial

This study compares two treatments for people with tight hamstring muscles (the muscles at the back of the thigh): instrument-assisted soft tissue mobilization (IASTM) and static stretching. Both are commonly used by physical therapists to improve flexibility, but few studies have looked at their effects beyond a few days after treatment ends.

Forty-six adults with hamstring tightness will be randomly assigned to one of two groups. One group will receive IASTM, and the other will receive static stretching. Both treatments will be given 3 times per week for 4 weeks (12 sessions total).

Researchers will measure flexibility (knee extension range of motion), pressure pain threshold, and physical performance (vertical jump and single-leg hop distance) at three time points: before treatment, 3 days after the last session, and 8 weeks after treatment ends. The goal is to find out which treatment provides better short-term and longer-term benefits.

Studieoversikt

Status

Har ikke rekruttert ennå

Detaljert beskrivelse

Hamstring muscle tightness is a common musculoskeletal condition that can limit hip and knee range of motion, reduce athletic and functional performance, and contribute to other conditions such as patellofemoral pain, patellar tendinopathy, and low back pain. Static stretching has long been used to address hamstring tightness, with systematic reviews suggesting that 6-8 weeks of regular stretching can produce lasting flexibility gains. Instrument-assisted soft tissue mobilization (IASTM) has more recently emerged as an alternative technique, with proposed mechanisms including controlled microtrauma that stimulates an inflammatory response and collagen remodeling in soft tissue.

Most existing studies comparing static stretching and IASTM for hamstring tightness have examined only single-session or short-term (immediate post-treatment) effects. Long-term follow-up data (≥8 weeks) are limited, making it difficult to determine whether treatment-related gains in flexibility, pain sensitivity, and functional performance are sustained over time.

This randomized controlled trial will enroll 46 participants with hamstring tightness, defined as hip flexion range of motion <65° on the Straight Leg Raise (SLR) test with no neurological signs. Participants will be randomly allocated (computer-generated randomization) to one of two equal groups (n=23 each):

Group 1 (IASTM): Participants will receive instrument-assisted soft tissue mobilization applied to the hamstring muscle group using a stainless-steel instrument, scanning technique, distal-to-proximal direction, for 5 minutes per session.

Group 2 (Static Stretching): Participants will receive manual static stretching of the hamstring muscle group, performed in 5 repetitions of 30 seconds of stretch followed by 30 seconds of rest (5 minutes total per session).

Both interventions will be delivered 3 times per week for 4 weeks (12 sessions total) by a physical therapist with over 10 years of clinical experience in orthopedic rehabilitation and manual therapy.

Outcome assessments will be performed by a blinded assessor independent of treatment delivery, at three time points: baseline (pre-treatment), short-term (3 days after the final session), and long-term (8 weeks after intervention completion). Outcome measures include:

  • Flexibility: knee extension range of motion during 90° hip flexion, measured with a digital inclinometer
  • Pressure pain threshold: measured with a digital algometer over the hamstring muscle bellies (biceps femoris, semitendinosus, semimembranosus)
  • Functional performance: vertical jump height and single-leg hop distance

Statistical analysis will include two-way repeated-measures ANOVA to assess time and group-by-time interaction effects, with Bonferroni-corrected post hoc comparisons where appropriate.

Studietype

Intervensjonell

Registrering (Antatt)

46

Fase

  • Ikke aktuelt

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  • Age 18 years or older
  • Hamstring tightness, defined as hip flexion range of motion <65° on the Straight Leg Raise (SLR) test, without neurological signs
  • No diagnosed chronic musculoskeletal or systemic disease
  • Signed informed consent form

Exclusion Criteria:

  • Previous trauma or surgical operation involving the lower extremity
  • Neurological symptoms radiating to one or both lower extremities due to hamstring injury, spinal pathology, or sciatic nerve involvement
  • Ankle instability
  • Pregnancy
  • Neurological signs elicited during the Straight Leg Raise (SLR) test
  • Hyperalgesia, hematoma, varicose veins, or active skin infection in the lower extremity

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Enkelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: IASTM

Participants will receive instrument-assisted soft tissue mobilization (IASTM) applied to the hamstring muscle group using a stainless-steel instrument in a scanning technique, distal-to-proximal direction, for 5 minutes per session, 3 times per week for 4 weeks (12 sessions total).

Participants will receive instrument-assisted soft tissue mobilization (IASTM) applied to the hamstring muscle group using a stainless-steel instrument in a scanning technique, distal-to-proximal direction, for 5 minutes per session, 3 times per week for 4 weeks (12 sessions total).

Aktiv komparator: Static Stretching

Participants will receive manual static stretching of the hamstring muscle group, performed in 5 repetitions of 30 seconds of stretch followed by 30 seconds of rest (5 minutes total per session), 3 times per week for 4 weeks (12 sessions total).

Participants will receive manual static stretching of the hamstring muscle group, performed in 5 repetitions of 30 seconds of stretch followed by 30 seconds of rest (5 minutes total per session), 3 times per week for 4 weeks (12 sessions total).

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in Knee Extension Range of Motion (Flexibility)
Tidsramme: Baseline, 3 days after final session (short-term), and 8 weeks after intervention completion (long-term)

Knee extension range of motion during 90° hip flexion, measured with a digital inclinometer, as an indicator of hamstring flexibility.

Baseline, 3 days after final session (short-term), and 8 weeks after intervention completion (long-term)

Samarbeidspartnere og etterforskere

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Sponsor

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. september 2026

Primær fullføring (Antatt)

1. februar 2027

Studiet fullført (Antatt)

1. februar 2027

Datoer for studieregistrering

Først innsendt

18. september 2026

Først innsendt som oppfylte QC-kriteriene

18. september 2026

Først lagt ut (Faktiske)

24. september 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

24. september 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

18. september 2026

Sist bekreftet

1. september 2026

Mer informasjon

Begreper knyttet til denne studien

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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