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Recruiting NCT07178873

NCT07178873 Psychosocial Teleassistance Programme for Adults With Spina Bifida

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Clinical Trial Summary
NCT ID NCT07178873
Status Recruiting
Phase
Sponsor University of Deusto
Condition Spina Bifida
Study Type INTERVENTIONAL
Enrollment 35 participants
Start Date 2024-06-25
Primary Completion 2027-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 75 Years
Study Type INTERVENTIONAL
Interventions
Psychosocial teleassistance intervention

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 35 participants in total. It began in 2024-06-25 with a primary completion date of 2027-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief 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 Criteria

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.

Contact & Investigator

Central Contact

Óscar Martínez, PhD

✉ oscar.martinez@deusto.es

📞 + 34 944 139 113

Frequently Asked Questions

Who can join the NCT07178873 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 75 Years, studying Spina Bifida. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07178873 currently recruiting?

Yes, NCT07178873 is actively recruiting participants. Contact the research team at oscar.martinez@deusto.es for enrollment information.

Where is the NCT07178873 trial being conducted?

This trial is being conducted at Bilbao, Spain.

Who is sponsoring the NCT07178873 clinical trial?

NCT07178873 is sponsored by University of Deusto. The trial plans to enroll 35 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology