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Mainz Outcome Predictor Studies: An Observational Clinical Trial Investigating Predictors for Postoperative Outcome

Mainz Outcome Predictor Studies: An Observational Clinical Trial Investigating Physiological and Psychological Data as Predictors for Postoperative Outcome.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01488617
Acronym
MOPS
Enrollment
616
Registered
2011-12-08
Start date
2012-01-31
Completion date
2013-10-31
Last updated
2013-10-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Psychological Distress, Surgery

Keywords

Surgery, Psychosocial Factors, Psychological Distress, Outcome Assessment (Health Care)

Brief summary

The purpose of this study is to determine whether psychological and social factors in addition to medical (physiological) conditions may contribute significantly to the prediction of the postoperative outcome. Postoperative outcome is defined (1) as postoperative complications and organ dysfunction and (2) alteration of quality of life.

Detailed description

Different factors contribute to the recovery process after surgical intervention. However, little is known about the predictive value of single factors. In addition to medical (physical) factors, depression, anxiety, somatization and avoiding coping styles are considered as relevant for the successful recovery process. These factors may be defined as psychological distress and could be used as predictors for perioperative complications and failed surgical treatment. Postoperative outcome is defined (1) as postoperative complications and organ dysfunction and (2) alteration of quality of life. Our sample includes adults undergoing extensive surgical interventions in trauma and orthopaedic surgery, urology, general surgery, and neurosurgery. The defined variables are measured using standardized and validated questionnaires prior to surgery and in follow-up visits.

Interventions

None listed

Sponsors

Johannes Gutenberg University Mainz
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Minimum Age 18 Years * German language in speaking and writing * Capability of giving consent * written informed consent

Exclusion criteria

* Delirium, dementia or other mental disorders with significant cerebral dysfunction * People under guardianship * simultaneous participation in other clinical studies

Design outcomes

Primary

MeasureTime frame
Quality of life6 weeks and 6 months after operation

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026