Onderzoek naar drie online zelfhulptrainingen voor slapen, stress en piekeren als aanpak van depressiepreventie.

Three online self-help interventions for sleep, stress and worry to prevent depression. A randomized effect study.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON22160

Enrollment

292

Registered

2014-05-27

Start date

2014-06-09

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

Sleep, stress, worry, depression, anxiety, well-being.

Interventions

Participants are randomised into: 1. Experimental condition 2. Waitlist control condition (with full access to usual care) Participants in the experimental condition have direct access to the onli

Eligibility

Inclusion criteria

Inclusion criteria: 1. 18 years and older; 2. experiences problems with sleep, stress or worry (subjective experience); 3. experiences mild to moderate depressive symptoms as determined with the Inventory of Depressive Symptomatology (IDS-SR, score 14-38); 4. has access to a computer with a solid Internet connection (the intervention and the questionnaires are offered online); 5. has an e-mail address; 6. has sufficient computer skills; 7. has sufficient Dutch language skills.

Exclusion criteria

Exclusion criteria: 1. experiences severe depressive symptoms as determined with the IDS-SR (score > 38); 2. has suicidal thoughts and/or plans as measured with item 18 from the IDS-SR; 3. experiences no depressive symptoms as determined with the IDS-SR (score < 14).

Design outcomes

Primary

Measure	Time frame
The primary outcome is: - Depression (Inventory of Depressive Symptomatology, time points: baseline, 3 months, 6 months)	—

Secondary

Measure	Time frame
- Depression (Inventory of Depressive Symptomatology, time points: baseline, 3 months, 6 months) - Anxiety (Generalized Anxiety Disorder Scale, time points: baseline, 3 months, 6 months) - Well-being (Warwick-Edinburgh Mental Well-being Scale, time points: baseline, 3 months, 6 months) - Cost-effectiveness (Trimbos/iMTA questionnaire for Costs associated with Psychiatric Illness, shortened version, time points: baseline, 3 months, 6 months) - Sleep (Jenkins Sleep Evaluation Questionnaire, time points: baseline, 3 months and 6 months); - Stress (Perceived stress scale, time points: baseline, 3 months, 6 months); or - Worry (Penn State Worry Questionnaire, time points: baseline, 3 months, 6 months).	—

Measure

Time frame

- Depression (Inventory of Depressive Symptomatology, time points: baseline, 3 months, 6 months) - Anxiety (Generalized Anxiety Disorder Scale, time points: baseline, 3 months, 6 months) - Well-being (Warwick-Edinburgh Mental Well-being Scale, time points: baseline, 3 months, 6 months) - Cost-effectiveness (Trimbos/iMTA questionnaire for Costs associated with Psychiatric Illness, shortened version, time points: baseline, 3 months, 6 months) - Sleep (Jenkins Sleep Evaluation Questionnaire, time points: baseline, 3 months and 6 months); - Stress (Perceived stress scale, time points: baseline, 3 months, 6 months); or - Worry (Penn State Worry Questionnaire, time points: baseline, 3 months, 6 months).

—

Contacts

Public ContactMarion Spijkerman

Universiteit Twente | Centre for eHealth and Wellbeing Research | Faculteit der Gedragswetenschappen | Vakgroep Psychologie, Gezondheid en Technologie |

m.p.j.spijkerman@utwente.nl053 - 489 6545

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)