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Evaluation and feasibility of an online support programme for breast cancer and head and neck cancer patients undergoing radiotherapy (OPUS)

Evaluation and feasibility of an online support programme for breast cancer and head and neck cancer patients undergoing radiotherapy (OPUS) - OPUS

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00031029
Enrollment
100
Registered
2023-01-18
Start date
2021-08-19
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

C00-C14 C30 C69 C50 C31 C33

Interventions

Group 1: Phase 1: development of OPUS Need Assessment T0: pre-survey in terms of a need assessment - questionaire: self implemented need assessment to establish disease and treatment related needs to

Sponsors

Nationales Centrum für Tumorerkankungen Dresden (NCT/UCC)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: patients - with head and neck as well as breast cancer diagnosis - having radiotherapy treatment at the university hospital dresden - that are linguistically, physically and mentally able to independantly handle an online programme - that are full-aged and able to consent - that are german as native language or native speaker level - having technical requirements to handle an online programme (web-enabled equipment) - written informed consent after a briefing about the project

Exclusion criteria

Exclusion criteria: patients - having insufficient knowledge of the german language - severe physical limitations (e.g. limited sight), that compromise the handling of an online support programme or is overcharging the patient - severe cognitive and/or linguistic limitations - limited capacity to contract - having a severe mental disorder Exclusion criteria are to be estimated by support therapists, as the circumstances require verified in the medical documentationsystem ORBIS or in exchange with the treating medical team

Design outcomes

Primary

MeasureTime frame
WHAT Is OPUS feasible for head and neck and breast cancer patients under radiotherapy? HOW Following domains were asked for in an interview after completing the online support programme: 1. technical and personal implementation 2. content aspects 3. graphical aspects 4. integration in clinical routine and radiation treatment concept 5. acceptance and adherence 6. completionrates WHEN T3

Secondary

MeasureTime frame
WHAT Does the OPUS tool have an effect on the psychological well-being, action competence and perceived self-efficiacy of head and neck and breast cancer patients? HOW Collect patient reported outcomes by use of standardised questionaires applying following parameters - psychological burden by use of NCCN Distress Thermometer (Mehnert, Müller, Lehmann, & Koch, 2006) - depressiveness and anxiety by use of Hospital Anxiety and Depression Scale (Zigmond & Snaith, 1983) - quality of life and symptom occurrence by use of EORTC QLQ-C30 (Aaronson et al., 1993) - Supportive Care Needs by use of Supportive Care Needs Survey (Lehmann, Koch, & Mehnert, 2012) WHEN T1, T2, T3, T4

Countries

Germany

Contacts

Public ContactTheresa Müller

Nationales Centrum für Tumorerkankungen Dresden (NCT/UCC)

Theresa.Mueller3@uniklinikum-dresden.de0351 458-19882

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026