Virtual Menstrual Pain Approaches in Females

NCT07497711 · Status: RECRUITING · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 145

Last updated 2026-05-20

No results posted yet for this study

Summary

This research study is testing two self-care approaches that may help prevent or reduce period pain in young females with primary dysmenorrhea, a common condition that causes painful menstrual cramps. Participants will be placed by chance into 1 of 3 groups: auricular acupressure, Baduanjin qigong, or a self-care education comparison group. The auricular acupressure and Baduanjin groups will receive online training and then practice the treatment on their own for 12 weeks. The main question is whether these two approaches can reduce the severity of menstrual pain. The study will also look at whether they can improve other symptoms that often happen with period pain, such as tiredness, poor sleep, anxiety, low mood, trouble concentrating, and reduced physical function. Researchers will also study stool and blood-related biological markers to better understand whether changes in gut bacteria and body metabolism may be linked to symptom improvement. A total of 145 participants will take part in the study at NTU, and any side effects or other safety concerns will be checked every week.

Conditions

  • Pain (Visceral, Somatic, or Neuropathic)
  • Women of Reproductive Age
  • Mental Disorder
  • Digital Health
  • Acupressure
  • Traditional Exercise
  • Host-Gut Microbiota Interaction
  • Metabolomics

Interventions

BEHAVIORAL

Virtual Auricular Acupressure

Virtual auricular acupressure involved acupuncturist-led virtual auricular acupressure treatment and self-administered application in this trial.

BEHAVIORAL

Virtual Baduanjin Qigong Exercise

Virtual Baduanjin Qigong Exercise involves instructor-led virtual exercise training and self-administered Baduanjin Qigong Exercise in this study.

BEHAVIORAL

Self Education

Attention Control with virtual training on menstrual hygiene and self-led menstrual health education.

Sponsors & Collaborators

  • Chengdu University of Traditional Chinese Medicine

    collaborator OTHER
  • Nanyang Technological University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
16 Years
Max Age
35 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-04-15
Primary Completion
2028-12-20
Completion
2029-03-20

Countries

  • Singapore

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07497711 on ClinicalTrials.gov