Skip to content

The effect of stretching exercise and cryotherapy in hamstring strain management

The effects of cryotherapy and cryostretch on clinical and functional outcomes in athletes with acute hamstring muscle strain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016030726957N1
Enrollment
37
Registered
2016-06-19
Start date
2016-04-29
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

muscle strain. Muscle strain

Interventions

Intervention 1: Superficial cooling by ice bag composed of crushed ice for intervention group(cryotherapy) 2. Intervention 2: Static stretching exercise of hamstring for intervention group(cryostretch
Rehabilitation
Superficial cooling by ice bag composed of crushed ice for intervention group(cryotherapy) 2
Static stretching exercise of hamstring for intervention group(cryostretch) 1

Sponsors

Vice chancellor for research,Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: The athletes participate in sports activity for at least two years and three times per week for a minimum of 2 hours each time? Male or female athlete between 18-40 years old? Athletes with acute first or second degree strain of hamstring; Pain evoked by resisted prone knee flexion and passive tension testing using? Participants are visited in sports physical therapy clinic within 72 hours after injury? Participants had no hypersensitivity or cold intolerance? participant had no sign of complete muscle disruption? no history of lower limb injury such as fracture or injury that required surgery within the past 6 months? No history of malignant or neurologic disease? No clinical finding showing radiculopathy? No hip flexor muscle shortness (as diagnose by Thomas test )? Participants agree not to take NSAID medication or receive any other form of treatment during the study. Exclusion criteria: If the patient dose not complete the treatment program and missing the sessions. The patient will stop his/her program any time he/she wants.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: On day 1 (before first treatment session) and day 6 (after fifth treatment session). Method of measurement: Visual Analog Scale (VAS).;Active and passive knee extension range of motion. Timepoint: On day 1 (before first treatment session) and day 6 (after fifth treatment session). Method of measurement: Knee extension test using inclinometer.;Functional status level. Timepoint: on day 1 (before first treatment session) and day 6 (after fifth treatment session). Method of measurement: Lower Extremity Functional Scale (LEFS).

Secondary

MeasureTime frame
_. Timepoint: _. Method of measurement: _.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNastaran Ghotbi

School of Rehabilitation Sciences, Tehran University of Medical Sciences

nghotbi@sina.tums.ac.ir+98 21 7753 3939

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026