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Feasibility of the YATAC Programme

The 'Young Adult Taking Action' Programme for Young Adult Cancer Survivors: a Feasibility Study Evaluating Content and Delivery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05551286
Acronym
YATAC
Enrollment
19
Registered
2022-09-22
Start date
2022-08-30
Completion date
2023-02-28
Last updated
2023-03-29

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

Conditions

Cancer

Keywords

Rehabilitation, Young adults

Brief summary

Young adult cancer survivors (YACS) aged 18-39 report physical and psychosocial late effects following cancer treatment, impairing quality of life and participation in everyday life. To address such multifactorial challenges complex or multicomponent rehabilitation interventions are needed. Based on this, the 'Young Adult Taking Action' (YATAC) programme was developed to increase participation in everyday life and improve health-related quality of life. The development of the intervention is guided by the British Medical Research Council's guidance (MRC) and the framework for the co-production and prototyping of public health interventions by Hawkins et al. The present study will investigate the acceptability and fidelity of the intervention at the research clinic of REHPA, the Danish Knowledge Centre for Rehabilitation and Palliative Care in Nyborg, Denmark. A mixed method one-armed feasibility study will be conducted and the results of the study will be used to revise version 1.0 of the programme.

Interventions

OTHERA rehabilition programme for young adult cancer survivors

The programme consists of 22 sessions focusing on; 1) everyday life (energy conservation, cognitive challenges, fatigue); 2) Physical activity; 3) psychological issues; 4) work and study d; 5) sexuality and relationship; 7) rights and finance, and 8) goal setting. The sessions include both education, workshops, and engagement in different activities and will be delivered by a multidisciplinary team.

Sponsors

Region of Southern Denmark
CollaboratorOTHER
University of Southern Denmark
CollaboratorOTHER
REHPA, The Danish Knowledge Centre for Rehabilitation and Palliative Care
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 39 Years
Healthy volunteers
No

Inclusion criteria

* Being between 18-39 years old at baseline * Have had any type of cancer * Have completed primary/active cancer directed treatment (cytotoxic chemotherapy, radiation therapy and/or definitive surgical intervention, while current hormonal treatments or maintenance therapies are permissible) * Determined a need for rehabilitation determined by the REHPA scale (a linear analogue scale, where the participants indicate how close they are to living the life they desire after ending cancer treatment). The scale ranges from 0= 'goal reached' to 9= 'infinitely far from' * Have access to a device with Internet options (i.e., smartphone or tablet)

Exclusion criteria

* Dependent in basic personal activities of daily living (personal care, dressing and eating) * No permanent residence in Denmark * Not able to speak and understand Danish

Design outcomes

Primary

MeasureTime frameDescription
Acceptability; Affective attitude10 weeksThe participants feelings about the intervention. Scores between 0-5, with higher scores indicating better feeling.
Fidelity10 weeksDefined as the consistency of whether the intervention was implemented as intended. The professionals register to what extent they have implemented the session as intended on a 5-point Likert scale. Scores between 0-5, with higher scores indicating higher consistency.
Dose10 weeksDefined as the quantity of intervention implemented. The professionals will report the number of elements implemented and the time used. In addition, the professional will give information on reasons for deviation from the manual.
Adaptions10 weeksDefined as any adjustments made to the intervention. The professionals register and describe any adaptions they make and the reasons for this.
Acceptability; burden10 weeksThe participants perceived amount of effort required to participate. Scores between 0-5, with higher scores indicating high degree of effort.
Acceptability; Ethicality10 weeksThe participants opinion about the intervention's fit with their individuals value system. Scores between 0-5, with higher scores indicating higher consistency with value system.
Acceptability; intervention cohesion10 weeksThe participants understanding of the intervention and how it works. Scores between 0-5, with higher scores indicating higher understanding of the intervention.
Acceptability; opportunity costs10 weeksThe participants experience of opportunity costs, like benefits, values, or profits that must be given up to engage in the intervention. Scores between 0-5, with higher scores indicating higher degree of giving up on opportunity costs, like benefits, values, or profits.
Acceptability; Perceived effectiveness10 weeksThe participants experience of perceived effectiveness of the intervention. Scores between 0-5, with higher scores indicating higher degree of perceived effectiveness of the intervention.
Acceptability; Self-efficacy10 weeksThe participants confidence that they can perform the behavior(s) required to participate in the intervention. Scores between 0-5, with higher scores indicating higher confidence that they can perform the behavior(s) required to participate in the intervention.

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026