Virtual Reality-Based Relaxation and Exergaming vs. Traditional Relaxation for Primer Dysmenorrhea

Trakya University

Status

Completed

Conditions

Primary Dysmenorrhea

Treatments

Behavioral: Non-immersive VR-Based Exergaming

Behavioral: Jacobson's Relaxation

Behavioral: Immersive Virtual Reality-Based Relaxation

Study type

Interventional

Funder types

Other

Identifiers

NCT06728306

TU-FTR-MŞY-002

1919B012219298 (Other Grant/Funding Number)

Details and patient eligibility

About

The goal of this clinical trial is to investigate the acute effects of virtual reality-based relaxation (immersive VR relaxation) and exergaming (non-immersive VR) compared to traditional Jacobson's relaxation on symptoms of primary dysmenorrhea (PD) in women aged 18-30 years with regular menstrual cycles. The main questions it aims to answer are:

Does immersive VR relaxation reduce abdomino-pelvic pain and menstrual symptom severity more effectively than Jacobson's relaxation? Does non-immersive VR exergaming provide better pain relief and symptom management compared to traditional relaxation methods?

Hypotheses:

Immersive VR relaxation will result in significantly greater reductions in abdomino-pelvic pain and menstrual symptom severity compared to traditional relaxation.

Non-immersive VR exergaming will also provide better outcomes in pain and symptom management compared to traditional relaxation.

Researchers will compare immersive VR relaxation, non-immersive VR exergaming, and Jacobson's relaxation (control group) to determine the relative effectiveness of each intervention.

Participants will:

Engage in a 20-minute session of one of the assigned interventions. Complete questionnaires on abdomino-pelvic pain, menstrual symptoms, and perceived effectiveness.

Participate in follow-up assessments for sleep quality during menstruation. This study aims to explore innovative, technology-driven approaches for managing menstrual symptoms and their effectiveness relative to traditional methods.

Full description

This study seeks to address this gap by investigating whether these innovative approaches can provide superior symptom relief. By evaluating pain intensity, symptom severity, and perceived effectiveness, this research will provide valuable insights into the feasibility and advantages of integrating technology into dysmenorrhea management.

Enrollment

43 patients

Sex

Female

Ages

18 to 30 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

women aged 18-30 with no pregnancy history.
a regular menstrual cycle (28 ± 7 days) over the past 6 months
menstrual pain with a Visual Analog Scale score >4 during this period

Exclusion criteria

regular medication use or medical treatment during the study (e.g., oral contraceptives, antidepressants).
recent musculoskeletal trauma or surgery.
intrauterine device use or pathological conditions/ultrasound findings of secondary dysmenorrhea
consumption of painkillers, alcohol, recreational drugs, or similar substances within the last 48 hours.