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ID
Source
Brief title
Health condition
Online health training versus no-treatment Control group.
Online gezondheidstraining versus een geen-behandeling Controlegroep
Sponsors and support
Intervention
Outcome measures
Primary outcome
The primary outcome measure is vitality, which consists of the standardized (z-scores) of the SVS and CIS.
Secondary outcome
Secondary study parameters include self-reported psychological outcome measures assessed at baseline, after 2 weeks, and after 4 weeks.
Background summary
The main aim of this study is to evaluate an abridged version of an online health training, based on cognitive behavioral therapy components, aimed at the optimization of health. Participants will be randomly allocated to either the Experimental group or the Control group and groups will be compared on psychological self-report measures after 2 weeks (immediately after the online health training), and at follow-up after four weeks, controlling for baseline.
Study objective
The aim of this study is to investigate an abridged version of an online health training, based on cognitive behavioral therapy components, that is focused on the optimization of health. It is expected that this online health training will have a significant positive effect on health parameters in a population of healthy people who show some potential to improve their health, as compared to a no-treatment Control group.
Study design
The study will take 4 weeks in total with measuring points at baseline, after 2 weeks, and after 4 weeks.
Intervention
A randomized controlled between-subjects design will be applied. Participants are randomly allocated to one of two groups: the Experimental group will receive the online health training of 2 weeks duration, while the Control group serves a no-treatment control group. Participant health parameters will be measured three times: at baseline, after 2 weeks, and at follow-up after four weeks.
PO Box 9555
A.W.M. Evers
Leiden 2300 RB
The Netherlands
+31 (0)71 527 3627
a.evers@fsw.leidenuniv.nl
PO Box 9555
A.W.M. Evers
Leiden 2300 RB
The Netherlands
+31 (0)71 527 3627
a.evers@fsw.leidenuniv.nl
Inclusion criteria
1. Healthy adults (based on demographic questions).
2. Between the ages of 18 and 35 years old.
3. A score of < 5 on the Subjective Vitality Scale (SVS: Ryan & Frederick, 1997) and/or a score of > 17 on the Checklist Individual Strength-Fatigue Severity Scale (CIS: Vercoulen et al., 1994).
Exclusion criteria
1. Severe medical or mental health conditions (based on demographics questions) that may interfere with the study protocol.
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
| Register | ID |
|---|---|
| NTR-new | NL5766 |
| NTR-old | NTR6008 |
| Other | Commissie Ethiek Psychologie (CEP) : CEP16-0218/70 |