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Evaluation of a Video-based Internet Intervention as Preparation for Inpatient Psychosomatic Rehabilitation

NCT02532881 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 492

Last updated 2016-11-15

No results posted yet for this study

Summary

The purpose of this study is to determine the effect of an internet-based preparation on the outcome expectancy and treatment credibility of rehabilitants concerning inpatient psychosomatic rehabilitation. Both study groups receive the usual written information for preparation (TAU). The patients of the experimental group have access to various videos on the study website until their inpatient rehabilitation begins, the patients of the placebo group receive no special treatment. The investigators hypothesize that the experimental group gains more positive outcome expectancy and treatment credibility compared to the control group.

Conditions

  • Outcome Expectancy

Interventions

OTHER

Videos

Various videos showing four characteristic patient stories and five expert statements on special topics concerning inpatient psychosomatic rehabilitation.

OTHER

Treatment as usual

Treatment as usual

Sponsors & Collaborators

  • University of Kaiserslautern-Landau

    collaborator OTHER

  • Deutsche Rentenversicherung

    collaborator OTHER

  • Johannes Gutenberg University Mainz

    lead OTHER

Principal Investigators

  • Rüdiger Zwerenz, Dr. · University Medical Center, Department of Psychosomatic Medicine and Psychotherapy, Johannes Gutenberg University Mainz

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-08-31
Primary Completion
2016-08-31
Completion
2016-10-31

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02532881 on ClinicalTrials.gov