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Psychosocial Teleassistance Programme for Adults With Spina Bifida

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.

ClinicalTrials.gov IDNCT07178873

PhaseNA

Enrollment35

SponsorUniversity of Deusto

Age18 Years

SexALL

I'm interested View official listing

Conditions studied

Spina Bifida, Self Esteem, Quality of Life (QOL), Self Concept, Anxiety, Depression, Interpersonal Needs

About this study

Interventions

Behavioral: 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.

Primary outcomes

Quality of life - The World Health Organization WHOQOL-BREF Quality of Life Assessment (3 months after the intervention)
Anxiety and depression - The Hospital Anxiety and Depression Scale (3 months after the intervention)
Depression - The Patient Health Questionnaire (3 months after the intervention)
Self-esteem - The Rosenberg Self-Esteem Scale (3 months after the intervention)
Self-Concept - Self-Concept Questionnaire Form-5 (3 months after the intervention)

Eligibility information

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.

Study locations

University of Deusto, Bilbao, Bizkaia 48007 Spain

Before you participate: Varda Clinical is an independent discovery tool, not the study sponsor or a medical provider. Eligibility can only be determined by the official study team. Discuss potential risks and benefits with a qualified healthcare professional.

Source: ClinicalTrials.gov. Record last refreshed by Varda Clinical: 2026-09-27.