Effectiveness of a guided web-based intervention for depression in back pain rehabilitation aftercare.

Effectiveness of a guided web-based intervention for depression in back pain rehabilitation aftercare. - WARD-BP

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00009272

Enrollment

210

Registered

2015-09-14

Start date

2015-12-01

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

F32.0 F32.1 F33.0 F33.1 M40-M54 R52.1 R52.2 G50-G59

Interventions

Group 1: Online-Training RückCare The intervention is based on Cognitive Behaviroal Therapy (CBT) including 6 weekly plus three optional modules and two booster sessions after end of intervention. Tra

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: a) age 18+ b) have back pain c) have a mild to moderate depression (PHQ = 5 and SCID ICD-10 F32.0/F32.1/F33.0/F33.1) d) not suicidal or suicidal attempts in the past e) medically suitable for participation f) sufficient knowledge of the German language g) sufficient computer und internet literacy for participation h) have internet access

Exclusion criteria

Exclusion criteria: a) current serve depression according to SCID (F32.2/F32.3/F33.2/F33.3)

Design outcomes

Primary

Measure	Time frame
Depression severity (HAM-D) at pre-treatment as well as 9 weeks and 6 months after randomisation.	—

Secondary

Measure	Time frame
Online survey at pre-treatment, as well as 9 weeks and 6 months after randomisation. health related quality of life (EQ-5D), depression response and remission (SKID, QIDS, PHQ-9), pain intensity (Rating scale), pain associated disability (ODI), working capacity (SPE), self-efficacy (PSEQ), satisfaction with the intervention (CSQ-8), side-effects of the intervention (INEP) and intervention adherence (attrition rate) as well as costs of the intervention (TiC-P)	—

Measure

Time frame

Online survey at pre-treatment, as well as 9 weeks and 6 months after randomisation. health related quality of life (EQ-5D), depression response and remission (SKID, QIDS, PHQ-9), pain intensity (Rating scale), pain associated disability (ODI), working capacity (SPE), self-efficacy (PSEQ), satisfaction with the intervention (CSQ-8), side-effects of the intervention (INEP) and intervention adherence (attrition rate) as well as costs of the intervention (TiC-P)

—

Countries

Germany

Contacts

Public ContactLasse Sander

Universität Freiburg, Abteilung Rehabilitationspsychologie und Psychotherapie

lasse.sander@psychologie.uni-freiburg.de07612033049

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 25, 2026