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Fibromyalgia, Cognitive Rehabilitation Software

S

Savaş Karpuz

Status

Begins enrollment this month

Conditions

Fibromyalgia
Cognitive Rehabilitation

Treatments

Device: cognitive rehabilitation with computer software

Study type

Interventional

Funder types

Other

Identifiers

NCT07010172
E-79735520-799

Details and patient eligibility

About

In recent years, especially in developed countries, FMS has emerged as a serious social problem by decreasing labour force and quality of life. Especially clinicians have started to consider cognitive dysfunction in FMS as a separate clinical condition. In the light of the data obtained, can say that cognitive dysfunction increases in the presence of depression, anxiety, sleep disorders, endocrine imbalances and pain.

Neuroscience and technological advances make it possible to meet the demand for care and improve the quality of stimulation by enabling the automation of many cognitive training procedures, improving patient record reliability and optimising performance of disability functions. The recently implemented RehaCom and HeadApp programmes (Schuhfried, Austria). excellent results have been reported in clinical practice with no significant adverse effects.

This study will investigate the effectiveness of a cognitive rehabilitation programme using computer software in female patients with fibromyalgia.

Enrollment

100 estimated patients

Sex

Female

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Being a woman
  • Diagnosed with fibromyalgia
  • 18-65 years old

Exclusion criteria

  • concomitant neurological disorder, learning disorder or cognitive impairment
  • current alcohol or recreational drug dependence or long-term (≥5 years) history of substance abuse
  • visual or hearing impairment that would interfere with cognitive testing
  • diagnosis of untreated obstructive sleep apnoea,
  • atypical sleep/wake patterns (e.g. night shift workers)
  • Lack of computer and internet access

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

100 participants in 1 patient group

cognitive rehabilitation software
Experimental group
Description:
3-5 sessions per week, 4 weeks cognitive rehabilitation with computer software
Treatment:
Device: cognitive rehabilitation with computer software

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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