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Development of a psychological expectancy training - phase 2: functionality and usability testing

Development of a psychological expectancy training - phase 2: functionality and usability testing - TRAIN-HEAL-TH-2

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON42999
Enrollment
10
Registered
2016-10-17
Start date
2017-08-09
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Het onderzoek wordt uitgevoerd onder patiënten met chronische aandoeningen die gepaard gaan met jeuk (zoals psoriasis of eczeem) en/of pijn (zoals reumatoïde artritis of fibromyalgie), en onder gezonde mensen. chronic pain or chronic itch

Interventions

Conditioning
eHealth
Health

Sponsors

Universiteit Leiden
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: For healthy volunteers: - age * 18 years - sufficient understanding of the Dutch language;For patients with a chronic pain or chronic itch condition: - age * 18 years - sufficient understanding of the Dutch language - confirmed diagnosis of chronic pain condition or chronic itch condition

Exclusion criteria

Exclusion criteria: For healthy volunteers: - confirmed diagnosis of chronic pain condition or chronic itch condition - severe physical or mental conditions (e.g., malignancy, psychosis, DSM-V diagnosis [American Psychiatric Association, 2013]) that interfere with the study protocol - pregnancy;For patients with a chronic pain or chronic itch condition: - severe physical or mental conditions (e.g., malignancy, psychosis, DSM-V diagnosis [American Psychiatric Association, 2013]) that interfere with the study protocol - pregnancy

Design outcomes

Primary

MeasureTime frame
The main study parameter of this pilot study is the usability of the eHealth and serious gaming intervention, assessed by questionnaires and semi-structured interviews using a think-aloud protocol during a single usability session at Leiden University (duration: 2 hours).

Secondary

MeasureTime frame
Not applicable.

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)