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Evaluation of scale ice on pain from dysmenorrhea in sedentary women

Analgesic efficacy of cryotherapy in sedentary women with primary dysmenorrhea

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-36vn7j
Enrollment
Unknown
Registered
2019-08-15
Start date
2019-07-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Primary dysmenorrhea

Interventions

Cryotherapy with a 1 kg scale ice pack was applied to 15 women of the experimental group in the lower abdomen region. The control group will also be composed of 15 women who will only perform the eval
Device
E02.258

Sponsors

Universidade Estadual do Oeste do Paraná (UNIOESTE)
Lead Sponsor
Universidade Estadual do Oeste do Paraná (UNIOESTE)
Collaborator

Eligibility

Sex/Gender
Female
Age
18 Years to 30 Years

Inclusion criteria

Inclusion criteria: Monthly condition of primary dysmenorrhea; have regular menstrual cycles; be between 18 and 30 years of age; be sedentary; agree to participate in the study

Exclusion criteria

Exclusion criteria: Use any other form of analgesia (such as analgesic drugs, analgesic electrical resources, physical exercises, among others); use anti-inflammatories; have secondary dysmenorrhea proven by medical examinations

Design outcomes

Primary

MeasureTime frame
The Brief Pain Inventory will be used, consisting of questions about the pain characteristic, location, intensity and changes in the daily activities that the pain produces; before starting the therapeutic procedures and at the end of the last session. A significant decrease in pain caused by the menstrual period is expected after the application of cryotherapy

Secondary

MeasureTime frame
No secondary outcomes are expected

Countries

Brazil

Contacts

Public ContactGladson Bertolini

Universidade Estadual do Oeste do Paraná (UNIOESTE)

gladson_ricardo@yahoo.com.br+55-045-32207344

Outcome results

None listed

Source: REBEC (via WHO ICTRP)