NCT07737145

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

65
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
794

participants targeted

Target at P75+ for all trials

Timeline
19mo left

Started Nov 2026

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 2, 2026

Completed
28 days until next milestone

First Posted

Study publicly available on registry

July 30, 2026

Completed
3 months until next milestone

Study Start

First participant enrolled

November 1, 2026

Expected
1.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2028

1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

May 31, 2028

Last Updated

July 30, 2026

Status Verified

July 1, 2026

Enrollment Period

1.5 years

First QC Date

July 2, 2026

Last Update Submit

July 29, 2026

Conditions

Keywords

Hospice carePalliative careIntimacyCommunicationCo-productionMixed methodsHealthcare professionalsEducationTrainingPerson-centred careSupport toolkitHospice service usersHolistic care

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.

Behavioral: Experience-Based Co-Design (EBCD) workshops

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.

Behavioral: Experience-Based Co-Design (EBCD) workshops

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.

Healthcare professionalsHospice service users

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

MeSH Terms

Conditions

Communication

Condition Hierarchy (Ancestors)

Behavior

Study Officials

  • Dr Kate Sugar

    Dorothy House

    PRINCIPAL INVESTIGATOR
  • Professor Candida McCabe

    Dorothy House

    STUDY CHAIR

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