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Effectiveness of different interventions in females with primary dysmenorrhea.

Effectiveness Of Different Interventions In Females With Primary Dysmenorrhea Among University Students. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/068340
Enrollment
200
Registered
2024-06-05
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: N944- Primary dysmenorrhea

Interventions

Intervention1: GROUP A : participants received conventional treatment for 3 days per week for 8 week Lifestyle advising & Exercising regularly , limiting caffeine ,sugar, alcohol intake , reduction o

Sponsors

Nisha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age 18 to 25 years 2.having a regular menstrual cycle (28–32 days) 3.having menstruation cramps 4.Suffering from primary dysmenorhea 5.Suffering from menstrual pain within the recent three consecutive months 6.no history of joint , motion ,muscle or bone diseases which reduce the ability to exercise 7.no history of mental and physical diseases

Exclusion criteria

Exclusion criteria: 1.Diagnosis of secondary dysmenorhea due to pelvic pathology, such as uterine fibroids, adenomyosis, endometriosis or pelvic inflammatory diseases. 2.Lactating, currently pregnant. 3.Taking no sedatives medications. 4.Pharmacology as a method of treatment. 5.Depressive or anxiety disorder, or use of psychiatric medication such as anti depressant. 6.Using an intra ?uterine contraceptive device (IUD) or taking oral contraceptive pills (OCP).

Design outcomes

Primary

MeasureTime frame
Pain Timepoint: At baseline and after the 8 week of intervention

Secondary

MeasureTime frame
Vas Msq WaliddTimepoint: At baseline & after the 8 week of intervention

Countries

India

Contacts

Public ContactNisha

Guru Jambheshwar University of Science & Technology

jyotisabharwal35@gmail.com9416665373

Outcome results

None listed

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