Feasibility of the YATAC Programme

Sponsor
REHPA, The Danish Knowledge Centre for Rehabilitation and Palliative Care (Other)
Overall Status
Recruiting
CT.gov ID
NCT05551286
Collaborator
Region of Southern Denmark (Other), University of Southern Denmark (Other)
20
1
1
5.1
4

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: A rehabilition programme for young adult cancer survivors
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
The 'Young Adult Taking Action' Programme for Young Adult Cancer Survivors: a Feasibility Study Evaluating Content and Delivery
Actual Study Start Date :
Aug 30, 2022
Anticipated Primary Completion Date :
Jan 31, 2023
Anticipated Study Completion Date :
Jan 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Young Adults Taking Action

The programme is person-centered, goal-oriented, and peer-based and is structured around a 5-day residential stay, an online follow-up after five weeks and a 2-day residential follow-up stay after ten weeks.

Other: A 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.

Outcome Measures

Primary Outcome Measures

  1. Acceptability; Affective attitude [10 weeks]

    The participants feelings about the intervention. Scores between 0-5, with higher scores indicating better feeling.

  2. Fidelity [10 weeks]

    Defined 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.

  3. Dose [10 weeks]

    Defined 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.

  4. Adaptions [10 weeks]

    Defined as any adjustments made to the intervention. The professionals register and describe any adaptions they make and the reasons for this.

  5. Acceptability; burden [10 weeks]

    The participants perceived amount of effort required to participate. Scores between 0-5, with higher scores indicating high degree of effort.

  6. Acceptability; Ethicality [10 weeks]

    The 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.

  7. Acceptability; intervention cohesion [10 weeks]

    The participants understanding of the intervention and how it works. Scores between 0-5, with higher scores indicating higher understanding of the intervention.

  8. Acceptability; opportunity costs [10 weeks]

    The 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.

  9. Acceptability; Perceived effectiveness [10 weeks]

    The participants experience of perceived effectiveness of the intervention. Scores between 0-5, with higher scores indicating higher degree of perceived effectiveness of the intervention.

  10. Acceptability; Self-efficacy [10 weeks]

    The 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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 39 Years
Sexes Eligible for Study:
All
Accepts 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 REHPA, The Danish Knowledge Centre for Rehabilitation and Palliative Care Nyborg The Region Of Southern Denmark Denmark 5800

Sponsors and Collaborators

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

Investigators

  • Principal Investigator: Maria Aagesen, PhD student, The University of Southern Denmark

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
REHPA, The Danish Knowledge Centre for Rehabilitation and Palliative Care
ClinicalTrials.gov Identifier:
NCT05551286
Other Study ID Numbers:
  • 1234
First Posted:
Sep 22, 2022
Last Update Posted:
Sep 22, 2022
Last Verified:
Sep 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by REHPA, The Danish Knowledge Centre for Rehabilitation and Palliative Care

Study Results

No Results Posted as of Sep 22, 2022