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Studying Non-motor Symptoms in HSP

U

University Hospital Tuebingen

Status

Completed

Conditions

SPG4

Treatments

Diagnostic Test: Brief Pain Inventory (BPI)
Diagnostic Test: EuroQol five dimensions questionaire (EQ-5D)
Diagnostic Test: Becks Depression Inventory (BDI)
Diagnostic Test: Restless-leg Questionaire (RLS diagnostic criteria)
Diagnostic Test: Modified Fatigue Impact Scale (MFI)

Study type

Observational

Funder types

Other

Identifiers

NCT03204773
NMS in HSP

Details and patient eligibility

About

Comparing the non-motor symptoms of patients with hereditary spastic paraplegia (HSP) to healthy controls (spouses, relatives or other healthy controls) by using the a number of specific questionaires

Full description

https://lamapoll.de/NMS_in_HSP

Enrollment

236 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Group 1: Patients with HSP (hereditary spastic paraplegia)
  • Group 2: Healthy controls
  • Age 18 to 70 years
  • Written, informed consent

Exclusion criteria

  • Lack of ability for a written, informed consent
  • Presence of spastic gait disorder or other neurological condition (Group 2)

Trial design

236 participants in 2 patient groups

HSP patients
Description:
Patients with hereditary spastic paraplegia regardless of their genetic mutation
Treatment:
Diagnostic Test: Modified Fatigue Impact Scale (MFI)
Diagnostic Test: EuroQol five dimensions questionaire (EQ-5D)
Diagnostic Test: Becks Depression Inventory (BDI)
Diagnostic Test: Restless-leg Questionaire (RLS diagnostic criteria)
Diagnostic Test: Brief Pain Inventory (BPI)
Healthy controls
Description:
healthy controls (spouses, relatives, or other healthy controls)
Treatment:
Diagnostic Test: Modified Fatigue Impact Scale (MFI)
Diagnostic Test: EuroQol five dimensions questionaire (EQ-5D)
Diagnostic Test: Becks Depression Inventory (BDI)
Diagnostic Test: Restless-leg Questionaire (RLS diagnostic criteria)
Diagnostic Test: Brief Pain Inventory (BPI)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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