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NCT04165473
A Training Program for Developing Social- and Personal Resources
trial testing Training Program for Developing Social- and Personal Resources in Stress, Psychological in 223 participants. Completed in 1 December 2024.
30 May 2023
Quick facts
| Lead sponsor | Medical University of Vienna |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 223 |
| Start date | 25 March 2023 |
| Primary completion | 30 May 2023 |
| Estimated completion | 1 December 2024 |
| Sites | 1 location across Austria |
Drugs / interventions tested
- Training Program for Developing Social- and Personal Resources
Conditions studied
- Stress, Psychological — all drugs for Stress, Psychological →
- Stress, Emotional — all drugs for Stress, Emotional →
- Health Behavior — all drugs for Health Behavior →
- Satisfaction, Personal — all drugs for Satisfaction, Personal →
Sponsor
Medical University of Vienna
Who can join
Adults 18 to 70, any sex, with Stress, Psychological or Stress, Emotional. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
In this study, a new psychosocial training for social relationships for adults will be evaluated. In a 6-module course, with four 3-day modules and two 5-day modules in the timeframe of one year, participants learn ways to strengthen their personal resources to establish effective social relationships and to develop skills as a social being. In between the module courses, the participants take 5 single sessions with an instructed trainer and document 10 conversations/social situations where they successfully apply the acquired personal and social skills. For my study, I will recruit a total of 200 persons. Approx. one hundred participants for the intervention group and 100 individuals for the control group. During the course of the training, the participants are taught social and personal skills that should result in a lower perceived stress level in daily life, improved health behaviour, a decreased presence of common somatic symptoms, a higher satisfaction with their lives, improved quality of their social relationships and a higher wellbeing. Data from study participants having accomplished additional training programs with the same training provider will be used to evaluate the influence on the results compared to participants without the extra addition for this study. The training participants will be assessed together with the controls. All study participants will be evaluated with standardized online questionnaires.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
The Relationship Between Body, Mind, and Social Characteristics in a Sample of a Training Program for Developing Social and Personal Resources: A Network Analysis.
Janka C, Höcker M, Dorner TE. · · 2024 · cited 1× · PMID 39767493 · DOI 10.3390/ijerph21121654 -
A Training Programme for Developing Social and Personal Resources and Its Effects on the Perceived Stress Level in Adults in Daily Life-Study Protocol for a Prospective Cohort Study.
Janka C, Stamm T, Heinze G, Dorner TE. · · 2022 · cited 1× · PMID 36612844 · DOI 10.3390/ijerph20010523
Verify or expand the search:
- PubMed search for NCT04165473
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04165473 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Medical University of Vienna
- Last refreshed: 26 March 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04165473.
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