TSK-C: measuring fear of movement in children and adolescents

TSK-C: measuring fear of movement in children and adolescents - TSK-C

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON30957

Enrollment

250

Registered

2007-05-04

Start date

2007-06-01

Completion date

Unknown

Last updated

2024-05-13

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

Conditions

kinesiofobia pain related fear

Interventions

None listed

Eligibility

Age

2 Years to 17 Years

Inclusion criteria

Inclusion criteria: Age between 8 and 16 years old patients: a-specific pain complaints

Exclusion criteria

Exclusion criteria: - non fluent in dutch - children in special education programs - patients: presence of chronic fatigue syndrome

Design outcomes

Primary

Measure	Time frame
De reliability of the TSK-C will be investigate by means of a confirmatory factor analyses. If the results are different from the adult version, reliability will be re-investigated by means of an exploratory factor analysis. The content validity of the TSK-C will be reviewed by experts on pain and fear of movement. The construct validity will be investigated by comparing the TSK-C to five other questionnaires, being the PCS-C, the STAIC, the FDI and the CDI-S. All questionnaires are expected to correlate significantly to each other. Finally, the healthy group will be compared to the patiënt group. It is expected that the patient group or a subgroup will show elevated scores on the TSK-C and other questionnaires. This will be tested by means of a students' t-test.	—

Measure

Time frame

De reliability of the TSK-C will be investigate by means of a confirmatory factor analyses. If the results are different from the adult version, reliability will be re-investigated by means of an exploratory factor analysis. The content validity of the TSK-C will be reviewed by experts on pain and fear of movement. The construct validity will be investigated by comparing the TSK-C to five other questionnaires, being the PCS-C, the STAIC, the FDI and the CDI-S. All questionnaires are expected to correlate significantly to each other. Finally, the healthy group will be compared to the patiënt group. It is expected that the patient group or a subgroup will show elevated scores on the TSK-C and other questionnaires. This will be tested by means of a students' t-test.

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Countries

Netherlands

Outcome results