Effectiveness and cost-effectiveness of a web-based routine assessment withintegrated recommendations for action for depression and anxiety (RehaCAT+)

Phase 3

Not yet recruiting

• Conditions: cardiological diseasesorthopaedic diseases; I00-I99; I00-I02; I05-I09; I10-I15; I20-I25; I26-I28; I30-I52; I60-I69; I70-I79

• Registration Number: DRKS00027447
• Lead Sponsor: niversität Ulm

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2022-01-11
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 1884

Inclusion Criteria

all orthopedic and cardiological rehabilitation patients with alleviated depression

Exclusion Criteria

none

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Depression severity 12 months after discharge from rehabilitation

Secondary Outcome Measures

Name	Time	Method
Anxiety severity, satisfaction with participation in social roles and activities, pain impairment, physical functioning, subjective quality of life, self-efficacy, fatigue, sleep quality, alcohol consumption, intervention adherence, health economic outcomes, utilization patterns, intervention acceptability, potential risks, and barriers and facilitators to implementation.