IN-TALK: Co-producing a Hospice Intimacy Support Toolkit in England
IN-TALK
Co-producing a Hospice Intimacy Support Toolkit to Enable Intimacy Needs Conversations in England
2 other identifiers
observational
794
0 countries
N/A
Brief Summary
People receiving hospice care may experience concerns about intimacy, closeness and physical affection that can affect their quality of life and wellbeing. However, healthcare professionals often report feeling uncertain about how to initiate or respond to conversations about intimacy needs. This can result in unmet needs and missed opportunities to provide holistic, person-centred care. The aim of the IN-TALK study is to co-produce a hospice intimacy support toolkit to support healthcare professionals in initiating and responding to conversations about intimacy needs with people receiving hospice care in England. This prospective mixed methods observational study uses Experience-Based Co-Design (EBCD) as its co-production methodology to develop a hospice intimacy support toolkit. Findings from the surveys will inform a series of co-production workshops involving hospice service users and healthcare professionals. Together, participants will co-produce the content and design of a hospice intimacy support toolkit to support person-centred care in hospice services across England.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Nov 2026
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 2, 2026
CompletedFirst Posted
Study publicly available on registry
July 30, 2026
CompletedStudy Start
First participant enrolled
November 1, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
April 30, 2028
Study Completion
Last participant's last visit for all outcomes
May 31, 2028
July 30, 2026
July 1, 2026
1.5 years
July 2, 2026
July 29, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Priorities for an intimacy support toolkit
Identification of priorities for the content, format and implementation of a hospice intimacy support toolkit through analysis of survey findings and Experience-Based Co-Design (EBCD) workshop discussions involving hospice service users and healthcare professionals.
Up to 24 months
Secondary Outcomes (2)
Hospice service users' intimacy support needs and priorities
During the cross-sectional survey data collection period (anticipated November 2026 to March 2027).
Healthcare professionals' confidence and educational needs
During the cross-sectional survey data collection period (anticipated April 2027 to September 2027).
Study Arms (2)
Hospice service users
Adults receiving hospice care in England who meet the study eligibility criteria and participate in the survey, the Experience-Based Co-Design (EBCD) workshops, or both, to inform the hospice intimacy support toolkit.
Healthcare professionals
Healthcare professionals working within hospice services in England who meet the study eligibility criteria and participate in the survey, the Experience-Based Co-Design (EBCD) workshops, or both, to inform the hospice intimacy support toolkit.
Interventions
Experience-Based Co-Design (EBCD) workshops are used as a co-production research method to collaboratively develop a hospice intimacy support toolkit with hospice service users and healthcare professionals. The workshops are part of the research methodology and are not a therapeutic or clinical intervention.
Eligibility Criteria
The study population comprises adult hospice service users (including patients, partners, loved ones and bereaved people receiving palliative and end of life care or support services from hospices in England) and registered and non-registered healthcare professionals working in hospices in England.
You may qualify if:
- Hospice service users: Aged 18 years or over. Hospice service users: Patients, partners, loved ones and bereaved people who are receiving, or have received, care or support services from hospices in England.
- Hospice service users: Able to understand and communicate in spoken and written English, independently or with the support of an interpreter.
- Hospice service users: Able and willing to provide informed consent. Healthcare professionals: Registered or non-registered healthcare professionals currently working within hospices in England involved in patient care and support.
- Healthcare professionals: Aged 18 years or over. Healthcare professionals: Able and willing to provide informed consent.
You may not qualify if:
- Hospice service users: Cognitive impairment that impedes communication. Healthcare professionals: Registered and non-registered Healthcare professionals currently working outside of hospices; and England.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Dorothy House Hospicelead
- St Oswald's Hospicecollaborator
- University of the West of England, Bristolcollaborator
- National Institute for Health and Care Researchcollaborator
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Dr Kate Sugar
Dorothy House
- STUDY CHAIR
Professor Candida McCabe
Dorothy House
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 2, 2026
First Posted
July 30, 2026
Study Start (Estimated)
November 1, 2026
Primary Completion (Estimated)
April 30, 2028
Study Completion (Estimated)
May 31, 2028
Last Updated
July 30, 2026
Record last verified: 2026-07