Spina BifidaSelf EsteemQuality of Life (QOL)Self ConceptAnxietyDepressionInterpersonal Needs
Investigational drug(s) / intervention(s)
Psychosocial teleassistance intervention
Psychosocial teleassistance intervention: The teleassistance psychosocial intervention involves 10 weekly 90-minute group sessions, with each group comprising 6 to 7 participants. These sessions are designed to enhance self-concept, self-esteem and social skills, reduce symptoms, and improve overall psychological well-being. Two follow-up sessions will be provided three months after the main program concludes.
Study summary
This clinical trial assesses the effect of a telecare psychosocial intervention designed for adults with spina bifida. The intervention consists of 10 weekly 1.5-hour group sessions, followed by two 3-month follow-up sessions. Each group will consist of 6 to 7 individuals. The intervention is aimed at strengthening aspects of self-concept, self-esteem, social skills and aims at a reduction of symptomatology and a general improvement of psychological well-being.
Eligibility
Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria:
* To be diagnosed with spina bifida by a specialist.
* Being between 18 and 75 years old.
* Having their informed consent or the informed consent of their legal guardians.
* Having Spanish as one of their main languages.
* Having access to a computer (with a camera, microphone and speakers integrated) and Internet connection to take part in the videoconferences.
Exclusion Criteria:
* Age that is inconsistent with the established range.
* The presence of any comorbid diagnosis or sensory deficit that would impede the effective execution of the intervention's activities.
Primary outcome measure(s)
Quality of life - The World Health Organization WHOQOL-BREF Quality of Life Assessment — 3 months after the intervention The World Health Organization WHOQOL-BREF Quality of Life Assessment (WHOQOL-BREF) is a tool designed to assess quality of life using twenty-six items. The questionnaire measures four different domains: physical health, psychological health, social relationships, and environment. Domain scores are transformed to a scale ranging from 0 to 100. Higher scores reflect better quality of life.
Anxiety and depression - The Hospital Anxiety and Depression Scale — 3 months after the intervention The Hospital Anxiety and Depression Scale (HADS) is a scale primarily designed to assess anxiety and depressive symptomatology using 14 items. The instrument is composed of two subscales: an anxiety subscale and a depression subscale. Total scores on each subscale range from 0 to 21, where a higher score is indicative of greater symptom severity.
Depression - The Patient Health Questionnaire — 3 months after the intervention The Patient Health Questionnaire (PHQ-9) is a brief, nine-item tool designed to detect and measure the severity of depression. The score can range from 0 to 27. Higher scores reflect more severe depressive symptoms, whereas lower scores indicate minimal or no depressive symptoms.
Self-esteem - The Rosenberg Self-Esteem Scale — 3 months after the intervention The Rosenberg Self-Esteem Scale (RSE) is a 10-item scale designed to assess self-esteem. The final score ranges from 10 to 40. Higher scores reflect greater self-esteem, whereas lower scores indicate reduced self-esteem.
Self-Concept - Self-Concept Questionnaire Form-5 — 3 months after the intervention The Self-Concept Questionnaire Form-5 (AF-5) is an instrument used to evaluate self-concept across five dimensions: social, academic-work/professional, emotional, family, and physical. Domain scores are transformed to a scale ranging from 0 to 10. Higher scores indicate a better self-concept across domains, while lower scores reflect worse self-concept in those areas.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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