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

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON23640

Enrollment

Registered

2016-03-17

Start date

2016-03-21

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

Online health training versus no-treatment Control group. Online gezondheidstraining versus een geen-behandeling Controlegroep

Interventions

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 dur

Eligibility

Inclusion criteria

Inclusion criteria: 1. Healthy adults (based on demographic questions). 2. Between the ages of 18 and 35 years old. 3. A score of 17 on the Checklist Individual Strength-Fatigue Severity Scale (CIS: Vercoulen et al., 1994).

Exclusion criteria

Exclusion criteria: 1. Severe medical or mental health conditions (based on demographics questions) that may interfere with the study protocol.

Design outcomes

Primary

Measure	Time frame
The primary outcome measure is vitality, which consists of the standardized (z-scores) of the SVS and CIS.	—

Secondary

Measure	Time frame
Secondary study parameters include self-reported psychological outcome measures assessed at baseline, after 2 weeks, and after 4 weeks.	—

Contacts

Public ContactA.W.M. Evers

LUMC PO Box 9555

a.evers@fsw.leidenuniv.nl+31 (0)71 527 3627

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)