search  
 


Home

Who are we?

Why
register?


Signup for
registration


Online registration

Log in to register
your trial


Search a trial

NRT en CCMO

Contact

NEDERLANDS





MetaRegister
van CCT (UK)


ISRCTN-Register
van CCT (UK)


The Effectiveness of an Online Health Training on Optimizing Health in a Healthy Population


- candidate number24122
- NTR NumberNTR6008
- ISRCTNISRCTN no longer applicable
- Date ISRCTN created
- date ISRCTN requested
- Date Registered NTR17-mrt-2016
- Secondary IDsCEP16-0218/70 Commissie Ethiek Psychologie (CEP)
- Public TitleThe Effectiveness of an Online Health Training on Optimizing Health in a Healthy Population
- Scientific TitleThe Effectiveness of an Online Health Training on Optimizing Health in a Healthy Population
- ACRONYMOptimize your Health
- hypothesisThe 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.
- Healt Condition(s) or Problem(s) studiedOnline Learning
- Inclusion criteria1. 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 criteria1. Severe medical or mental health conditions (based on demographics questions) that may interfere with the study protocol.
- mec approval receivedyes
- multicenter trialno
- randomisedyes
- masking/blindingNone
- controlPlacebo
- groupParallel
- Type2 or more arms, randomized
- Studytypeintervention
- planned startdate 21-mrt-2016
- planned closingdate21-jun-2016
- Target number of participants60
- InterventionsA 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.
- Primary outcomeThe primary outcome measure is vitality, which consists of the standardized (z-scores) of the SVS and CIS.
- Secondary outcomeSecondary study parameters include self-reported psychological outcome measures assessed at baseline, after 2 weeks, and after 4 weeks.
- TimepointsThe study will take 4 weeks in total with measuring points at baseline, after 2 weeks, and after 4 weeks.
- Trial web siten/a
- statusplanned
- CONTACT FOR PUBLIC QUERIESProf. Dr. A.W.M. Evers
- CONTACT for SCIENTIFIC QUERIESProf. Dr. A.W.M. Evers
- Sponsor/Initiator Leiden University
- Funding
(Source(s) of Monetary or Material Support)
Leiden University Medical Center (LUMC)
- Publicationsn/a
- Brief summaryThe 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.
- Main changes (audit trail)
- RECORD17-mrt-2016 - 29-sep-2016


  • Indien u gegevens wilt toevoegen of veranderen, kunt u een mail sturen naar nederlands@trialregister.nl