Skip to content

COMPARING DRY CUPPING AND HOT MOIST PACK FOR SEVERE MENSTRUAL PAIN IN FEMALE ATHLETES

Comparative effect of dry cupping and hot moist pack on primary dysmenorrhea and cardiovascular parameters in female athletes: A randomized clinical trial. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/096764
Enrollment
56
Registered
2025-11-03
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

None listed

Interventions

Intervention1: dry cupping therapy: dry cupping therapy will be given for first 3days of menstrual cycle for 3 consecutive months (at abdomen pr lowback) Control Intervention1: hot moist pack: hot mos

Sponsors

KAHER Institute of Physiotherapy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Female athletes [nulliparous) Training commitment for 3 or more organized sessions weekly (for more than150 minutes structured sport participation) Regular menstrual cycles with confirmed primary dysmenorrhea history Pain intensity, On activity more than5, At rest more than 3 on VAS Willingness to abstain from analgesic medications more than 6 hours prior to testing Provision of written informed consent Andreson and Milsom grade more than grade 2

Exclusion criteria

Exclusion criteria: Secondary dysmenorrhea conditions (endometriosis pelvic pathology) Pregnancy or breastfeeding status Bleeding disorders anticoagulant therapy or skin infections at potential cupping sites Cardiovascular or neurological disorders Medications affecting heart rate parameters Contraindications to dry cupping therapy and hot moist pack Inability to maintain supine/prone positioning for 30-40 minutes

Design outcomes

Primary

MeasureTime frame
VAS [visual analogue scale] pain intensity rating and Andreson and Milsom grade Timepoint: VAS [visual analogue scale] pain intensity rating and Andreson and Milsom grade will be taken before and after the intervention that is at day 1 of start of the intervention and after 3 months once the intervention is over

Secondary

MeasureTime frame
Resting heart rateTimepoint: Resting heart rate 60-second measurement wil be taken for each participant before anf after the intervention ;Blood pressure Timepoint: Blood pressure (average of 2 readings) will be taken before nad after the intervention;pulse rateTimepoint: will be measure before and after the intervention;Menstrual distress questionnaire [MCQ]Timepoint: will be taken before and after the intervention , it has 3 sections and will be scored out of 78 as mild, moderate and severe distress;Perceived performance scaleTimepoint: will be taken before and after the intervention;Simple Attendance LogTimepoint: will be taken before and after the intervention

Countries

India

Contacts

Public ContactSrushti Chavan

KAHER Institute of Physiotherapy

sanjanapammannavar@klekipt.edu.in9380358281

Outcome results

None listed

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