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Acupressure, sleep and fatigue in students with Premenstrual Syndrome

Phase 1
Conditions
Premenstrual syndrome.
Premenstrual Tension Syndrome
Registration Number
IRCT201206126247N6
Lead Sponsor
Vice Chancellor for Research, Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
140
Inclusion Criteria

students with fatigue and sleep quality score of 31 and 5, respectively; regular menstruation of 24-35 days; age between 18-35 years old; not married; no physical and mental diseases; no medication or traditional treatment for controlling Premenstrual Syndrome (PMS);
Exclusion criteria: Unwillingness to continue participation in the trial; performing incomplete acupressure for less than 6 consecutive days for any reason; irregular menstruation; get married during the trial; pharmacological or non-pharmacological treatments for Premenstrual Syndrome during the trial.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sleep Quality and Fatigue. Timepoint: pre and post intervention (before and after acupressure). Method of measurement: Fatigue Severity Scale (FSS) and Pittsburg Sleep Quality Index (PSQI).
Secondary Outcome Measures
NameTimeMethod
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