Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
46 participants
INTERVENTIONAL
2025-03-06
2025-08-30
Brief Summary
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Purposes: To investigate the effectiveness of multimedia-guided acupressure at the Sanyinjiao acupoint in improving primary dysmenorrhea among young women.
Research method: This study employs a quasi-experimental pretest-posttest design over a three-month period. Participants will be recruited from two selected colleges in central Taiwan through voluntary enrollment. It is anticipated that each group, experimental and control, will consist of 22 participants. The experimental group will receive general multimedia health education videos along with self-made multimedia videos teaching acupressure at the Sanyinjiao acupoint. Treatment will commence one week before the menstrual cycle and continue until the 5th day of menstruation. On the other hand, the control group received general multimedia health education videos only.
Results: The data will be analyzed by SPSS 28.0 statistical software. Statistical methods will include descriptive statistics such as frequency, percentage, mean, and standard deviation analysis. Inferential statistics will include independent t-tests, chi-square tests, and paired t-tests to compare menstrual pain conditions before and after the intervention and the differences between the two groups.
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Detailed Description
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Purposes: To investigate the effectiveness of multimedia-guided acupressure at the Sanyinjiao acupoint in improving primary dysmenorrhea among young women.
Research method: This study employs a quasi-experimental pretest-posttest design over a three-month period. Participants will be recruited from two selected colleges in central Taiwan through voluntary enrollment. It is anticipated that each group, experimental and control, will consist of 22 participants. The experimental group will receive general multimedia health education videos along with self-made multimedia videos teaching acupressure at the Sanyinjiao acupoint. Treatment will commence one week before the menstrual cycle and continue until the 5th day of menstruation. On the other hand, the control group received general multimedia health education videos only.
Results: The data will be analyzed by SPSS 28.0 statistical software. Statistical methods will include descriptive statistics such as frequency, percentage, mean, and standard deviation analysis. Inferential statistics will include independent t-tests, chi-square tests, and paired t-tests to compare menstrual pain conditions before and after the intervention and the differences between the two groups.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Multimedia-Guided Acupressure at Sanyinjiao for Primary Dysmenorrhea
Intervention: Self-Acupressure (Multimedia-Guided)
Self-Acupressure
Both groups received general health education videos. The experimental group performed SP6 acupressure starting one week before menstruation, 10 minutes per session, twice daily, until the fifth day of menstruation. The control group maintained their usual routines.
Control Group
The control group maintained their usual routines
No interventions assigned to this group
Interventions
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Self-Acupressure
Both groups received general health education videos. The experimental group performed SP6 acupressure starting one week before menstruation, 10 minutes per session, twice daily, until the fifth day of menstruation. The control group maintained their usual routines.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
2. Pregnant or breastfeeding women;
3. History of gynecological surgery;
4. Contraindications to acupoint massage, such as thrombocytopenia with bleeding tendency, local infection or inflammation at the massage site, excessive weakness, etc.;
5. Already capable of using acupoint massage to relieve pain;
6. Students enrolled in the course taught by the principal investigator.
18 Years
30 Years
FEMALE
Yes
Sponsors
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China Medical University, Taiwan
OTHER
Responsible Party
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Cheng, Jui-Fen
Associate Professor
Principal Investigators
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Jui-Fen Cheng
Role: PRINCIPAL_INVESTIGATOR
China Medical University, China
Central Contacts
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Other Identifiers
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CMUH113-REC3-133
Identifier Type: -
Identifier Source: org_study_id
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