KontextSucht – Rehabilitation for Dependency Patients with and without their Accompanying Children in Germany

KontextSucht – Rehabilitation for Dependency Patients with and without their Accompanying Children in Germany - KontextSucht

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00030950

Enrollment

790

Registered

2023-01-25

Start date

2023-04-01

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

F10-F19

Interventions

Group 1: The study population will include German speaking, substance abusing parents with children until the age of 14. All study participants need to participate in the intervention. The clinic pers

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: German language knowledge Parent of a child </=14 years

Exclusion criteria

Exclusion criteria: Discontinued treatment

Design outcomes

Primary

Measure	Time frame
The aim of the accompanying study is as a first step to conduct a feasibility study and as a second step a benefit assessment of the intervention. Abstinence of the study participants should further lead to social and professional participation. The goal of the intervention and at the same time the study outcome is to improve abstinence, parenting skills, educational behaviour and the relationship between child and parent. Data collection will be conducted with qualitative interviews and quantitative, standardised questionnaires (e.g. PSS by Büssing, 2011). During the feasibility study quantitative and qualitative data will be collected at the end of the 12-week long intervention. The longitudinal study design of the benefit assessment uses the survey dates t1 at the beginning of the intervention, t2 at the end of the intervention and t3 one year after the intervention for both, qualitative and quantitative data collection. The collected qualitative data will be analysed using qualitative content analyses by Mayring with use of “MAXQDA”. Quantitative data will be analysed descriptively and inductively with the help of the “R for data science” software.	—

Measure

Time frame

The aim of the accompanying study is as a first step to conduct a feasibility study and as a second step a benefit assessment of the intervention. Abstinence of the study participants should further lead to social and professional participation. The goal of the intervention and at the same time the study outcome is to improve abstinence, parenting skills, educational behaviour and the relationship between child and parent. Data collection will be conducted with qualitative interviews and quantitative, standardised questionnaires (e.g. PSS by Büssing, 2011). During the feasibility study quantitative and qualitative data will be collected at the end of the 12-week long intervention. The longitudinal study design of the benefit assessment uses the survey dates t1 at the beginning of the intervention, t2 at the end of the intervention and t3 one year after the intervention for both, qualitative and quantitative data collection. The collected qualitative data will be analysed using qualitative content analyses by Mayring with use of “MAXQDA”. Quantitative data will be analysed descriptively and inductively with the help of the “R for data science” software.

—

Secondary

Measure	Time frame
social and professional participation	—

Countries

Germany

Contacts

Public ContactAnanda Stullich

Technische Universität München (TUM)

ananda.stullich@tum.de+49 89 289 24198

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 9, 2026