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HYPNOflow – Hypnotherapeutic Audio Intervention for Reducing Anxiety and Restlessness During Urodynamic Examinations

HYPNOflow – Hypnotherapeutic Audio Intervention for Reducing Anxiety and Restlessness During Urodynamic Examinations

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00038537
Enrollment
40
Registered
2025-11-24
Start date
2026-01-13
Completion date
Unknown
Last updated
2026-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Children who require an outpatient urodynamic study for medical reasons. Typical conditions include spina bifida, posterior urethral valves, and other congenital or urological disorders.

Interventions

Group 1: Children who require an outpatient urodynamic study for medical reasons (including the placement of a transurethral bladder catheter and measurement of bladder pressure during bladder filling

Sponsors

Klinik für Kinderchirurgie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 18 Years

Inclusion criteria

Inclusion criteria: Children aged 3 to 18 years who undergo a urodynamic examination for medical reasons.

Exclusion criteria

Exclusion criteria: Lack of consent or unwillingness to participate in the study; children with sensory or cognitive comorbidities that would make participation impossible.

Design outcomes

Primary

MeasureTime frame
Measured anxiety and stress of the children before, during, and after the examination using the SAM test, SUD, and mYPAS-SF.

Secondary

MeasureTime frame
Impact of the perceived anxiety and stress on the quality and evaluability of the urodynamic examination (number of artefacts, interpretability of findings, whether the measurement could be completed successfully). Impact of parental perceived anxiety (STAI-State) on the children’s anxiety.

Countries

Germany

Contacts

Public ContactFriederike Heidtmann

Klinik für Kinderchirurgie

Friederike.heidtmann@med.uni-Jena.de036419322772

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 14, 2026