Social Learning Theory-Based Menstruation Education in Visually Impaired Women
The Effectiveness of Social Learning-Based Planned Education on Menstruation in Visually Impaired Young Women
The aim of this study is to evaluate the effect of face-to-face practical training based on social learning theory on developing and changing skills and behaviors in providing genital and menstrual hygiene and improving menstrual self-care skills of visually impaired young women.
Our hypotheses are:
H1: There is a difference between the mean Menstruation Symptom Questionnaire scores of the intervention group at the pre- and post-training follow-ups.
H2: There is a difference between the mean Genital Hygiene Behaviors Scale scores of the intervention group at the pre- and post-training follow-ups.
H3: There is a difference between the mean Menstruation Symptom Questionnaire scores of the intervention and control groups at the post-training follow-ups.
H4: There is a difference between the mean Genital Hygiene Behaviors Scale scores of the intervention and control groups at the post-training follow-ups.
H5: The mean Menstrual Self-Care Skill List scores of the intervention group after the training were higher than before the training. Researchers compared the knowledge and behavioral changes of the experimental and control groups after the training.
Participants did the following:They fully participated in the planned training, performed the skill applications, and answered the survey questions completely. They were expected to apply the knowledge and skills they learned in the training in their daily lives for 9 months. At the end of the 9th month, a follow-up interview was conducted, and an attitude assessment was performed.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Izmir, Turquía (Türkiye)
- Ege university
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Niño
- Adulto
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Female participants aged 15-30 years
- For totally blind participants: visual acuity of 20/200 or less in the better eye and/or a visual field of 20 degrees or less
- For low vision participants: visual acuity between 20/70 and 20/200 in the better eye
- Having experienced menstruation at least once
- No other disabilities, such as hearing or orthopedic impairments
- Voluntary participation with informed consent
Exclusion Criteria:
- Amenorrhea due to systemic or metabolic conditions (e.g., hypogonadotropic hypogonadism, hypothyroidism, hyperthyroidism, Turner syndrome)
- Visual conditions such as night blindness, color blindness, or monocular blindness that do not meet the defined visual impairment criteria
- Incomplete participation in the training or follow-up phases
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Investigación de servicios de salud
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
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Experimental: Intervention Group
Participants in the intervention group received a structured, face-to-face, half-day education based on Bandura's Social Learning Theory.
The training included verbal explanation, modeling, interactive games, tactile materials, and audio-described educational videos.
The content focused on menstrual symptoms, genital hygiene behaviors, and menstrual self-care skills.
Education was designed to be accessible for visually impaired participants.
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This is a structured, face-to-face menstrual and hygiene education program based on Bandura's Social Learning Theory, developed for visually impaired young women.
The intervention aims to improve menstrual self-care skills, genital hygiene behaviors, and symptom management.
The training includes verbal instruction, modeling, reinforcement techniques, tactile materials, and audio-described educational videos.
Interactive games and small-group activities (max 4 participants) are used to support engagement and skill development.
Each session lasts approximately half a day (3-4 hours).
Educational content was reviewed by experts and piloted for accessibility.
The program addresses cognitive, behavioral, and sensory learning needs to support independent menstrual hygiene management in visually impaired women.
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Sin intervención: Control Group
Participants in the control group did not receive any training.
Only data collection was performed using the same forms and at the same time points as the intervention group.
They were blinded to group allocation.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
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Menstruation Symptom Questionnaire
Periodo de tiempo: Baseline and 9 months after intervention
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Developed by Chesney and Tasto (1975) to assess menstrual pain and symptoms, the scale was updated by Negriff et al. (2009) by re-evaluating its factor structure and usability in adolescents.
Turkish validity and reliability were established by Güvenç et al. (2014).
The scale is a 5-point Likert-type scale consisting of 22 items.
Participants are asked to rate their menstrual symptoms on a scale of 1 (never) to 5 (always).
The scale consists of three sub-dimensions: Negative Effects/Somatic Complaints (Items 1-13), Menstrual Pain Symptoms (Items 14-19), and Coping Mechanisms (Items 20-22).
The lowest possible score is 22, and the highest is 110.
The average of the total scores obtained from the items on the scale provides the scale score.
An increase in the average score indicates an increase in the severity of menstrual symptoms.
The score obtained from the sub-dimensions of the scale is calculated by calculating the average total score of the item
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Baseline and 9 months after intervention
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Genital Hygiene Behavior Scale
Periodo de tiempo: Baseline and 9 months after intervention
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Genital Hygiene Behavior Scale Developed by Karahan in 2017, this scale measures women's genital hygiene behaviors.
It consists of three sub-dimensions: "General Hygiene " (12 items), "Menstrual Hygiene" (8 items), and " abnormal finding awareness" (3 items).
The minimum scale score is 23, and the maximum is 115.
The scale has 23 items, using a five-point Likert scale.
Items are rated from "strongly agree = 5" to "strongly disagree = 1".
As the score on the scale increases, the rate at which women exhibit correct genital hygiene behavior also increases.
The Cronbach's alpha values for the scale are 0.80 for "Genital Hygiene Behaviors Scale", 0.70 for "Genital Hygiene Habits", 0.74 for "Menstrual Hygiene", and 0.8 for " abnormal finding awareness", respectively (Karahan, 2017).
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Baseline and 9 months after intervention
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Menstrual Self-Care Skills Checklist
Periodo de tiempo: Evaluated before and immediately after the intervention.
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The researcher prepared this skills checklist based on the literature. It consists of three sections: Menstruation Tracking Skills, Pad Changing Skills, and Genital Hygiene Skills. "No" is scored as "0", "Partially knowing" as "1", and "Yes" as "2". Expert evaluation was obtained to assess the content validity of the checklists. Menstruation Tracking Skills; There are 7 items related to knowing the signs that menstruation, determine the day menstruation will begin, knowing the duration of menstrual bleeding, the frequency of menstruation, monitoring bleeding, and noticing pad fullness. The Pad Changing Skill consists of eight items in total. The steps are: removing the soiled pad from the underwear, removing and discarding the packaging of the clean pad, placing the clean pad into the underwear, and securing it to the underwear. Genital Hygiene Skills; This section includes seven items related to hand washing and genital cleaning. |
Evaluated before and immediately after the intervention.
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Özlem Demirel Bozkurt, Associate Professor, PhD, RN, Ege University Nursing Faculty
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- AYLINOLGUN_VISUALLYIMPAİRMENT
- 125S056 (Otro número de subvención/financiamiento: The Scientific and Technological Research Council of Türkiye (TÜBİTAK))
- 1219/1199 (Otro identificador: İzmir Bakırçay University Non-Interventional Clinical Research Ethics Committee)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
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