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An online self-management intervention for patients with fibromyalgia -- a randomised controlled trial

An online self-management intervention for patients with fibromyalgia -- a randomised controlled trial - Online self-management in fibromyalgia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON55570
Enrollment
70
Registered
2016-11-30
Start date
2017-01-25
Completion date
Unknown
Last updated
2024-06-11

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

Conditions

fibromyalgie fibromyalgia (FM) fibromyalgia syndrome (FMS)

Interventions

The intervention is based on cognitive-behavioral methods. It starts off with a face-to-face introduction consultation in which personal goals for the intervention are set. Subsequently, the tailore
in between are four modules aimed at learning how to cope with the consequences of a chronic condition in daily life. The modules focus on (1) activity, (2) mood, (3) thoughts, and (4) the social en

Sponsors

Universiteit Leiden
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Diagnosed with fibromyalgia, as previously confirmed by their treating GP or a medical specialist - Pain complaints with a minimal duration of 3 months - Minimum age of 18 years - Fluent in Dutch language - Able to give informed consent - Own a computer with internet access

Exclusion criteria

Exclusion criteria: - Difficulties in (written) communication (e.g., due to analphabetism) - Severe physical and psychiatric comorbidities that interfere with the study protocol, such as psychosis, addiction, suicidal ideation - On-going psychological treatment elsewhere - Participation in other clinical trials - Pregnancy

Design outcomes

Primary

MeasureTime frame
The primary outcome will be pain coping, measured with a VAS score.

Secondary

MeasureTime frame
As secondary outcomes, a number of other psychological and physical outcome measures will be assessed (e.g., HR-QoL, well-being, pain impact on daily life, pain cognitions), as well as quality of the therapeutic relationship and cost-effectiveness of the intervention.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)