Effects of Dry Heat Application for Menstrual Symptoms

The study was conducted as a randomized controlled trial, a non-blinded between 30 September 2019 and 29 November 2019. In the first stage of the present study, the Premenstrual Syndrome Scale was used for all participants and the study was continued with the students with premenstrual syndrome symptoms based on the data acquired from the Premenstrual Syndrome Scale. This stage was used only for restricting the sample group, rather than diagnosing or treating the students. In the second stage, the randomization of students included in the sample group was presented according to the CONSORT diagram. The population of the study consisted of 452 female nursing students studying in the faculty of health sciences in a university. The students (n=75) who were absent in the school, took analgesics during the study, and did not agree to participate in the study, were excluded from the study. The students, who had no diagnosis of psychiatric disorder and history of endometriosis, stated that they menstruated regularly (between 22-35 days), did not use complementary and alternative treatments such as analgesics or massage throughout the study, had no diabetes or neuropathic problem causing nerve injury, did not take oral contraceptives, were over 18 years, and agreed to participate in the study, were included in the study.

Inclusion criteria

• having no diagnosis of psychiatric disorder and history of endometriosis
• stated that they menstruated regularly (between 22-35 days),
• not use complementary and alternative treatments such as analgesics or massage throughout the study,
• having no diabetes or neuropathic problem causing nerve injury,
• not take oral contraceptives,
• were over 18 years,
• agreed to participate in the study

Exclusion criteria

• analgesics during the study
• not agree to participate in the study