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A Smartphone App for Women With Primary Dysmenorrhea

Evaluation of a Smartphone Application for Self Care for Women With Menstrual Pain (Primary Dysmenorrhea): a Randomized Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03432611
Acronym
smartAID
Enrollment
594
Registered
2018-02-14
Start date
2018-02-19
Completion date
2021-03-31
Last updated
2019-07-31

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

Conditions

Primary Dysmenorrhea

Keywords

mHealth, dysmenorrhea, acupressure, self-management, self-care

Brief summary

With a randomized, pragmatic study the effectiveness of a smartphone app for menstrual pain in 18-34-year-old women with primary dysmenorrhea will be investigated.

Detailed description

Smartphone apps may be useful to guide and support individuals in self-management strategies. Primary dysmenorrhea is a very common problem for women. With a randomized, pragmatic study the investigators aim to evaluate whether a smartphone app for women with menstrual pain is effective in reducing menstrual pain in 18-34-year-old women with primary dysmenorrhea. For this the investigators compare the complete smartphone app with two control versions of this app. The complete app provides evidence-based self-care information and instructions for self-acupressure in menstrual pain, the control intervention I includes self-care information, but no instructions for self-acupressure, and control intervention II includes instructions for self-acupressure, but no self-care information. The investigators aim to observe 594 women with primary dysmenorrhea over 12 menstruation cycles. The primary outcome is the mean pain intensity on the days with pain during the 6th menstruation after randomization using a numerical rating scale (NRS; 0=no pain; 10=strongest pain imaginable). Women are eligible when they suffer from primary dysmenorrhea, are between 18 and 34 years old, not pregnant and do not plan to be pregnant within the next 12 months.

Interventions

OTHERSelf-care information feature

The self-care feature offers information on self-care for menstrual pain. The following topics are shown: exercise, dietary supplementation, heating pad/hot water bottle, yoga, and information on when to consult a doctor and how primary dysmenorrhoea is often treated. Notifications from the app which can be deactivated remind women of surveys and activities.

OTHERSelf-acupressure feature

The acupressure feature offers detailed written and multimedia descriptions of an acupressure used for menstrual pain. Three acupressure points are described, which should be massaged bilaterally twice a day up to five times a day on the 5 days before menstruation and during menstruation. Each point should be massaged for 2 minutes. A timer for the acupressure and notifications from the app which can be deactivated remind women of surveys and acupressure.

Sponsors

University of Zurich
CollaboratorOTHER
Charite University, Berlin, Germany
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

randomized, three-armed pragmatic study

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 34 Years
Healthy volunteers
No

Inclusion criteria

* Female, aged 18-34 years * Dysmenorrhea, defined as self-reported menstrual cramps or pain during every menstrual cycle which started during the teenage years * No prior history of a gynecological disease that is known to be a reason for the dysmenorrhea * Not more than 5 days with menstrual pain outside the menstrual period itself * Menstruation within the last six weeks and a cycle length of 3 to 6 weeks * Moderate or severe pain, defined as a score equal to or higher than 6 on a numeric rating scale (NRS, 0 to 10) for the worst pain intensity during the last menstruation * Informed consent * Possession of an iPhone * Willingness and ability to input and share anonymous data through the study app * The willingness to see a doctor when 1) pain is getting worse than usual, 2) pain medication is not helping, and 3) when the pain is still present well before or well after the period.

Exclusion criteria

* Known pregnancy * Pregnancy already planned for the forthcoming 12 months

Design outcomes

Primary

MeasureTime frameDescription
Mean pain intensity on the days with painDaily during the 6th menstruation after randomizationThe mean pain intensity on the days with pain during the 6th menstruation after randomization using a numerical rating scale (NRS; 0=no pain; 10=strongest pain imaginable).

Secondary

MeasureTime frameDescription
ResponderDaily during menstruation (1st to 12th menstrual cycles)Responder defined as having at least 50% pain reduction on the days with pain
Number of days with pain (duration of pain)Daily during menstruation (1st to 12th menstrual cycles)Number of days participants reported pain.
Days with absence from work, training, or studiesBaseline, end of menstruation (1st to 12th menstrual cycles)Days with absence from work or education because of menstrual pain during previous period.
Days with pain medicationDaily during menstruation (1st to 12th menstrual cycles)Days with intake of pain medication for menstrual pain during each menstruation
Mean pain intensity on the days with painBaseline; daily during menstruation (1st to 5th and 7th to 12th menstrual cycles)The mean pain intensity on the days with pain during the menstruation 1 to 5 and 7 to 12 after randomization using a numerical rating scale (NRS; 0=no pain; 10=strongest pain imaginable).
Severe adverse eventsEnd of menstruation (3rd, 6th, 9th, and 12th menstrual cycles)Characteristics and duration of severe adverse events
Frequency of acupressure application5 days before menstruation and during menstruation (1st to 12th menstrual cycles)Number of times acupressure was applied during each cycle
User satisfactionEnd of menstruation (1st to 12th menstrual cycles)User's satisfaction with app guided activity (NRS; 0=totally unsatisfied; 6=very satisfied)
Adverse reactionEnd of menstruation (1st to 12th menstrual cycles)Characteristics of adverse reaction

Countries

Germany

Contacts

Primary ContactDaniel Pach, MD
daniel.pach@charite.de004930450529068
Backup ContactIris Bartsch
iris.bartsch@charite.de004930450529132

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026