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NCT Number: NCT07010172

Fibromyalgia, Cognitive Rehabilitation Software

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.

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Key information

Conditions

Fibromyalgia Cognitive Rehabilitation Muscular Diseases Musculoskeletal Diseases Nervous System Diseases Neuromuscular Diseases Rheumatic Diseases

Age range

18 year–65 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

cognitive rehabilitation with computer software

Device

3-5 sessions per week, 4 weeks cognitive rehabilitation with computer software

Primary outcomes

  1. Stroop Colour and Word Test

    Time frame: start and first month

  2. Number Range Test

    Time frame: start and first month

Secondary outcomes

  1. modified Fibromyalgia impact questionnaire

    Time frame: start and first month

Sponsors and collaborators

Lead sponsor

Savaş Karpuz

Other Gov

Registry information

Official study title

Effectiveness of Cognitive Rehabilitation Software in Female Patients With Fibromyalgia

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jun 8, 2025
Registry last updated
Jun 8, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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