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NCT05828693Completed

Systemic Stress Prevention Via Application SysLife© for Companies

Efficacy of Systemic Stress Prevention Via Application SysLife© for Companies: A Randomized Controlled Feasibility Study

Source: ClinicalTrials.gov · Last updated 8 May 2024

Brief summary (registry, in English)

The purpose of this study is to investigate the efficacy of systemic stress prevention via SysLife© application in a prospective, interventive, balanced, monocentric, explanatory pilot randomized controlled trial (RCT), with participants' subjective stress experience as the primary endpoint. Research Question: Which implementations are necessary, based on the experience from this pilot RCT, to ensure the quality of a subsequent confirmatory RCT? Hypothesis: We expect improvement of participants' subjective stress experience, goal achievement, systemic functioning in private and organisational social systems while using the SysLife© application.

Status (registry)
Completed
Study type
Interventional
Enrollment
49 (actual)
First submitted
12 Dec 2022
Start date
29 Jan 2023
Primary completion date
1 Mar 2024
Lead sponsor
University of Witten/Herdecke
NCT number
NCT05828693

What you commit to

  • Study type: Interventional
  • Participants enrolled: 49
  • From 29 Jan 2023 to the primary completion date, 1 Mar 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • No written consent

Who the study is looking for

  • Minimum age: 18 years
  • Interest in active use of the SysLife© application
  • Knowledge of German at native language level or the ability to use German language independently (at least B-level)
  • Only persons capable of giving consent will be included in the study
  • Written consent to participate after information about the study

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Witten/Herdecke University
Coordinator of this site? Confirm its status
WittenGermanyUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.