Implementation and evaluation of the online self-help intervention "This is your life" in primary care: A pretest-posttest study

Implementation and evaluation of the online self-help intervention "This is your life" in primary care: A pretest-posttest study - Implementation and evaluation of "This is your life" in primary care

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON43295

Enrollment

Registered

2016-03-29

Start date

2016-04-25

Completion date

Unknown

Last updated

2024-04-23

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

Conditions

iedereen die last heeft van lichamelijke klachten en een verminderd welbevinden Physical symptoms and low or moderate well-being

Interventions

All participants have free access to the online self-help intervention "This is your life", following completion of the baseline assessment. This self-help intervention is focused on strengthening p

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - The participant is 18 years or older. - The participant has chronic somatic symptoms of any kind. - The participant experiences low to moderate well-being, as determined by the Mental Health Continuum-Short Form (MHC-SF). - The participant has access to a computer, laptop or tablet/iPad with an adequate Internet connection. - The participant possesses an e-mailadress. - The participant has sufficient computer skills. - The participant is motivated to complete at least 4 lessons of the online self-help intervention in a 3-month period. - The participant is able to read and write Dutch. - The participant provides informed consent.

Exclusion criteria

Exclusion criteria: - The participant experiences a high level of well-being (flourishing), as determined by the Mental Health Continuum-Short Form (MHC-SF). - Presence of moderate to serious depressive or anxiety symptoms: score >14 on the depression scale and/or score >14 on the anxiety scale of the Hospital Anxiety and Depression Scale (HADS).

Design outcomes

Primary

Measure	Time frame
The primary outcome is the level of well-being, measured with the MHC-SF.	—

Secondary

Measure	Time frame
Secondary outcomes are resilience (BRS), depression (HADS-D), anxiety (HADS-A), positive and negative affect (PANAS), use of talents (SUS), self-compassion (SCS-SF) and positive relations (subscale of the PGGS). Additional variables include socio-demographic characteristics (i.e. sex, age, nationality, marital status, work- and living situation, education) and symptom-related characteristics (e.g. type of symptoms, time, received care).	—

Measure

Time frame

Secondary outcomes are resilience (BRS), depression (HADS-D), anxiety (HADS-A), positive and negative affect (PANAS), use of talents (SUS), self-compassion (SCS-SF) and positive relations (subscale of the PGGS). Additional variables include socio-demographic characteristics (i.e. sex, age, nationality, marital status, work- and living situation, education) and symptom-related characteristics (e.g. type of symptoms, time, received care).

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Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)