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Fibromyalgia, Cognitive Rehabilitation Software

Effectiveness of Cognitive Rehabilitation Software in Female Patients With Fibromyalgia

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07010172
Enrollment
100
Registered
2025-06-08
Start date
2025-07-01
Completion date
2026-08-01
Last updated
2025-06-08

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

Conditions

Cognitive Rehabilitation, Fibromyalgia

Brief summary

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.

Interventions

DEVICEcognitive rehabilitation with computer software

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

Sponsors

Savaş Karpuz
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Stroop Colour and Word Teststart and first month
Number Range Teststart and first month

Secondary

MeasureTime frame
modified Fibromyalgia impact questionnairestart and first month

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026