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.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Réel)
Phase
- N'est pas applicable
Contacts et emplacements
Lieux d'étude
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Izmir, Turquie (Türkiye)
- Ege university
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Enfant
- Adulte
Accepte les volontaires sains
La description
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 d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Recherche sur les services de santé
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Seul
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
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Expérimental: 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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Aucune intervention: 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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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Menstruation Symptom Questionnaire
Délai: 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
Délai: 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
Délai: 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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Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Özlem Demirel Bozkurt, Associate Professor, PhD, RN, Ege University Nursing Faculty
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- AYLINOLGUN_VISUALLYIMPAİRMENT
- 125S056 (Autre subvention/numéro de financement: The Scientific and Technological Research Council of Türkiye (TÜBİTAK))
- 1219/1199 (Autre identifiant: İzmir Bakırçay University Non-Interventional Clinical Research Ethics Committee)
Plan pour les données individuelles des participants (IPD)
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Informations sur les médicaments et les dispositifs, documents d'étude
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