Effect Review of orange spring notes and isometric training on primary dysmenorrhea and sleep quality of non-athletic female students at Shahrood University of Technology

The effect of iranian spring and isometric exercise on primary dysmenorrhea and sleep quality of non-athletic female students at Shahrood University of Technology;The four groups are: Fluorouracil: Training group: Practice group and Basal group: Control group.

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190302042878N1

Enrollment

Registered

2021-05-18

Start date

2019-02-23

Completion date

Unknown

Last updated

2021-05-26

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

Conditions

Dysmenorrhea.

Interventions

Intervention 1: "Intervention group:" only the orphan spring was used, "tarting an intervention from a week before the menstruation until the fifth day of the menstruation for 12 days and the method o

Eligibility

Sex/Gender

Female

Age

18 Years to 24 Years

Inclusion criteria

Inclusion criteria: Iranian and resident of Shahrood dormitories Single Regular menstrual period Non-athlete

Exclusion criteria

Exclusion criteria: Marriage Irregular chemotherapy Pelvic diseases

Design outcomes

Primary

Measure	Time frame
Fradi, who had a pain intensity of more than 4 at a visual pain scale, were included in the research. Timepoint: Before the intervention and immediately after the intervention. Method of measurement: Visual Analogue Scale: In order to measure pain in subjects, a visual analog scale, or a pain reliever, was used which includes a horizontal line that is scaled from zero to 10, and zero indicates absolute analgesia and 10 signs of unbearable pain. . The degree of pain was measured by the researcher using a visual-linear pain measurement scale that was standardized to measure pain severity. Measured. For this purpose, the person is asked to determine the severity of pain in the area of ??the affected body by selecting one of the numbers between 1-10, or selecting one of the smears designed (painless, mild pain, moderate pain, severe pain, Most pain possible. The subjects were accordingly divided into 4 groups without primary dysmenorrhea (0). Mild primary dysmenorrhea (1-3). Median Primary Dysmenorrhea( 4-6). And severe.	—

Measure

Time frame

Fradi, who had a pain intensity of more than 4 at a visual pain scale, were included in the research. Timepoint: Before the intervention and immediately after the intervention. Method of measurement: Visual Analogue Scale: In order to measure pain in subjects, a visual analog scale, or a pain reliever, was used which includes a horizontal line that is scaled from zero to 10, and zero indicates absolute analgesia and 10 signs of unbearable pain. . The degree of pain was measured by the researcher using a visual-linear pain measurement scale that was standardized to measure pain severity. Measured. For this purpose, the person is asked to determine the severity of pain in the area of ??the affected body by selecting one of the numbers between 1-10, or selecting one of the smears designed (painless, mild pain, moderate pain, severe pain, Most pain possible. The subjects were accordingly divided into 4 groups without primary dysmenorrhea (0). Mild primary dysmenorrhea (1-3). Median Primary Dysmenorrhea( 4-6). And severe.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Hasani

Shahrood University of Technology

hassani-3@yahoo.com+98 23 3239 2204

Outcome results

None listed

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