Subjective Spine Value: Efficient Evaluation of Spinal Function

Subjective Spine Value: Efficient Evaluation of Spinal Function - SSpV

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00035389

Enrollment

308

Registered

2024-11-14

Start date

2024-11-14

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

Scoliosis (juvenile scoliosis, adolescent scoliosis, congenital scoliosis, secondary scoliosis, degenerative scoliosis, asymptomatic subjects)

Interventions

Group 1: Healthy Participants (No Scoliosis) as Control Group Additional questionnaires in addition to the study-independent treatment according to the standard of the spine center (see section Prima

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Scoliotic deformity of the spine

Exclusion criteria

Exclusion criteria: No consent from the patient or legal guardian possible Inability to adequately answer questionnaire items (e.g., language barrier, patient’s age)

Design outcomes

Primary

Measure	Time frame
As part of this observational study, spinal function will be assessed using questionnaires (Subjective Spine Value (SSpV), Oswestry Disability Index (ODI), Core Outcome Measures Index for the back (COMI-back), Scoliosis Research Society Score (SRS-22r)) in addition to standard treatment procedures administered independently of the study by the spine center over a 2-year period. Assessments will be conducted preoperatively as well as postoperatively (at 2-4 weeks, 12 weeks, 6 months, and 1 year). Data collection will occur as part of medically indicated treatment or via email.	—

Measure

Time frame

As part of this observational study, spinal function will be assessed using questionnaires (Subjective Spine Value (SSpV), Oswestry Disability Index (ODI), Core Outcome Measures Index for the back (COMI-back), Scoliosis Research Society Score (SRS-22r)) in addition to standard treatment procedures administered independently of the study by the spine center over a 2-year period. Assessments will be conducted preoperatively as well as postoperatively (at 2-4 weeks, 12 weeks, 6 months, and 1 year). Data collection will occur as part of medically indicated treatment or via email.

—

Secondary

Measure	Time frame
Anthropological Data (age, sex, BMI, …) Secondary Diagnoses/Findings (obesity, malnutrition; in case of prior surgery: screw loosening, material fracture, …) Radiological Data (Cobb angle, lumbar modifier, Lenke classification, …)	—

Countries

Germany

Contacts

Public ContactBernhard Hoehl

Charité-Universitätsmedizin Berlin

bernhard.hoehl@charite.de+4930450652474

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026