Intervention to Support Partners and Informal Caregivers of Frail RA-patients

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorGlostrup University Hospital, Copenhagen

About this trial

Background Rheumatoid arthritis (RA) is a chronic inflammatory disease associated with pain, fatigue, functional limitations, and reduced quality of life. As more people live to older age with RA, age-related vulnerability such as frailty becomes increasingly relevant and may amplify functional decline, multimorbidity, and reliance on others. Informal caregivers (unpaid family members, friends, or neighbors) often provide substantial practical, emotional, and coordination support, yet caregiver needs are frequently overlooked in rheumatology care. INSPIRE (INtervention to Support Partners and Informal caREgivers of frail RA patients) is an individually tailored support intervention developed using the UK Medical Research Council framework for complex interventions and an iterative co-creation process involving older adults with RA and frailty, caregivers, healthcare professionals, and social care stakeholders. Before a definitive evaluation, feasibility and acceptability in routine care must be established.

Aim To evaluate the feasibility and acceptability of delivering INSPIRE in routine rheumatology care and to test study procedures in preparation for a future definitive trial.

Methods This is a single-arm feasibility study recruiting 25 informal caregivers of older adults with RA and frailty. Recruitment will occur within a fixed four-month window (1 March-1 July 2026) and will not be extended. Care recipients (older adults) will be ≥65 years with RA and frailty classified as Clinical Frailty Scale (CFS) 4-7. Caregivers will be ≥18 years, provide unpaid support, and report at least moderate burden defined as a Caregiver Burden Scale (CBS) mean score \>1.99 at screening. Participants will be recruited from Rigshospitalet (Center for Rheumatology and Spine Diseases) and rheumatology departments in Køge, Slagelse, and Holbæk. Identification uses routine patient-reported outcomes (DANBIO) with invitation of potentially frail patients (e.g., MDHAQ \>1.0) followed by telephone screening and CFS assessment; eligible patients nominate a caregiver who is then screened using CBS.

Intervention INSPIRE is delivered by a trained healthcare professional over \~12 weeks and comprises three contacts: an initial consultation (60-90 min), a brief follow-up (15-30 min), and a final consultation (30-60 min). Content is tailored using a toolbox addressing validation of the caregiver role, emotional/practical support, education, communication, and navigation across health and municipal services. Involvement of the older adult in consultations is optional and based on preferences of both parties.

Outcomes Feasibility outcomes include recruitment (screened/eligible/consented), retention at 12 weeks, questionnaire completeness, and deliverability (session completion, mode, duration). Acceptability will be assessed post-intervention using the Acceptability of Intervention Measure and supplemented by brief acceptability/feasibility questions and qualitative interviews. Fidelity and tailoring will be documented using structured session notes. Exploratory outcomes include caregiver burden measured by Caregiver burden scale, quality of life measured by WHOQOL-BREF (caregiver and older adult), and physical function measured by MDHAQ .

Progression criteria Pre-specified criteria include approximately 50% recruitment of those approached, ≥85% retention, and high fidelity, reviewed using a trafficlight approach (go/amend/stop).

Ethics and dissemination Written informed consent will be obtained from both the older adult and the caregiver prior to baseline data collection, with separate consent for any study components each participant takes part in (e.g., consultations, interviews). Findings will be disseminated through peer-reviewed publication, conferences, and stakeholder summaries.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Informal (unpaid) caregiver of an older adult with confirmed rheumatoid arthritis (RA)

Aged ≥ 18 years

Care recipient aged ≥ 65 years

Able to provide informed consent

Disqualifiers

Severe cognitive impairment preventing participation

Acute mental health crisis

Other circumstances making it impracticable to complete the intervention and follow-up assessments

Trial design

Design model

Single group

Treatments tested in this trial

  • Caregiver support

    Behavioral

    Intervention: INSPIRE INSPIRE is delivered by a trained healthcare professional with rheumatology expertise and experience in psychosocial support and service navigation. The intervention runs over approximately twelve weeks and includes an initial consultation, follow-up, and a final consultation. The initial consultation (about 60-90 minutes) takes place at home or in the clinic and is guided by the caregiver's CBS pro-file. It focuses on recognizing and validating the caregiver role, identifying the most burdensome is-sues, exploring underlying causes, and establishing realistic goals. Based on the needs identified, the caregiver is introduced to a tailored toolbox of resources and referral pathways that may include emotional or psychological support options, guidance on managing practical and physical strain, support for social isolation, communication and relationship support, disease-related education, and assistance navigating municipal and health system services.

Treatment groups

25 Participants
are divided into 1 treatment group
Group A: Support interventionExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Recruitment rate

Recruitment rate will be assessed as the number of caregivers recruited out of the number of eligible caregivers

Time frame
3 months
2

Retention rate

Retention rate will be assessed as the number of participants who withdrew from the study out of the total number of participants.

Time frame
3 months
3

Intervention deliverability

Number of sessions completed

Time frame
3 months
4

Intervention deliverability

Session duration

Time frame
3 months

Secondary outcomes

1

Fidelity

Intervention fidelity is estimated based on documentation sheets, filled out after each session by the healthcare professional delivering the intervention

Time frame
3 months
2

Data completeness

Missing data will be assessed as the number of items answered relative to the total number of items (i.e., item-level completeness)

Time frame
3 months
3

Acceptability

Acceptability will be assessed using post-intervention acceptability questions

Time frame
3 months
4

Caregiver burden

The Caregiver Burden Scale (CBS) is a 22-item self-report questionnaire covering five domains (general strain, isolation, disappointment, emotional involvement, and environment). Each item is rated on a 4-point response scale from 1 to 4, yielding a mean total score ranging from 1 (minimum) to 4 (maximum). Higher scores indicate worse outcome (greater perceived caregiver burden).

Time frame
Baseline and 3 months

Other outcomes

Sponsors and contacts

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