LTC: The Living With a Long-Term Condition Study

Sponsor
King's College London (Other)
Overall Status
Recruiting
CT.gov ID
NCT06072287
Collaborator
(none)
600
1
6.4
93.2

Study Details

Study Description

Brief Summary

Psychological distress (anxiety and depression) is common in and experienced differently by people living with long-term health conditions (LTCs). Being able to measure whether psychological distress is related to living with a LTC would allow researchers and clinicians to provide interventions specifically tailored to the challenges of living with a LTC and therefore provide the most appropriate support for these patients. Such a measure would also be useful in research to identify the presence of illness-related distress in different patient groups. This project will therefore create a new measure of illness-related distress that has applications for both research and clinical practice. This will involve the psychometric validation of the new illness-related distress measure to test how valid and reliable the measure is.

The aim of the project is to provide initial validation of the Illness Related Distress Scale in a community sample, recruited through online platforms. The objective of the study is to gather initial validity and reliability data for the scale.

Detailed Description

Background: see brief summary

Project information:

This study will be conducted online with participants from the UK. A series of standardised questionnaires will be used alongside the new questionnaire.

Participants will be those who self-select to complete our survey by responding to advertisements. The invitation will include a link to the Qualtrics survey which includes the Participant Information Sheet, Eligibility Screening, Consent Form and Baseline Questionnaire.

After completing eligibility screening and consent, participants will complete the baseline questionnaire which will include brief demographics (highest education level, long-term condition diagnoses, ethnicity age and gender), the new measure we are testing (the Illness Related Distress Scale), as well as the Patient Health Questionnaire (PHQ-8), Generalised Anxiety Disorder Scale (GAD-7), the Work and Social Adjustment Scale (WSAS). The baseline questionnaire will only include the Inflammatory Bowel Disease Distress Scale (IBD-DS) and Diabetes Distress Scale (DDS) if participants indicate that they have a diagnosis of the relevant condition.

At 1 week follow-up, participants will be sent a Qualtrics link to complete our 1-week follow-up questionnaire which will include the new Illness-Related Distress Scale only.

Participants:

We are aiming to recruit 600-700 participants for the study.

Study Design

Study Type:
Observational
Anticipated Enrollment :
600 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Testing the Reliability and Validity of a New Measure for Illness-related Distress.
Actual Study Start Date :
Jun 28, 2023
Anticipated Primary Completion Date :
Dec 31, 2023
Anticipated Study Completion Date :
Jan 10, 2024

Arms and Interventions

Arm Intervention/Treatment
Participants

Participants will answer two short questionnaires, 1 week apart.

Diagnostic Test: Living with LTC Questionnaire
A questionnaire that will ask about demographic information, mental wellbeing and distress related to chronic illness.

Outcome Measures

Primary Outcome Measures

  1. Illness-related distress [Week 0 and Week 1]

    31 item questionnaire developed by the research team designed to assess illness-related distresss.

Secondary Outcome Measures

  1. Depression [Week 0]

    Eight-item Patient Health Questionnaire - 8 (PHQ-8) Minimum=0, maximum=24, with higher scores indicating greater depression.

  2. Anxiety [Week 0]

    Seven-item Generalised Anxiety Disorder Scale (GAD-7). Minimum=0, maximum=21, with higher scores indicating greater anxiety.

  3. Functional impairment [Week 0]

    Five-item Work and Social Adjustment Scale (WSAS). Minimum=0, maximum=50, with higher scores indicating greater functional impairment.

  4. Diabetes Related Distress Scale [Week 0]

    Diabetes Related Distress Scale (DDS-17), a 17 item self-report diabetes related distress questionnaire. Minimum=17, maximum=102, with higher scores indicating greater distress.

  5. IBD Distress Scale [Week 0]

    IBD Distress Scale, a 28 item self-report IBD related distress questionnaire. Minimum=29, maximum=145, with higher scores indicating greater distress.

  6. Cognitive and Behavioural Responses to Symptoms [Week 0]

    Cognitive Behavioural Responses to Symptoms Questionnaire, 40 item self-report questionnaire consisting of seven subscales with items scored on a 5 point scale. Higher scores correspond with stronger presence of the specific cognitive/behavioural response. The seven subscales refer to 1) fear avoidance, 2) catastrophising, 3) damage beliefs, 4) embarassment avoidance 5) symptom focussing 6) all-or-nothing behaviour and 7) avoidance/resting behaviour.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Over the age of 18

  • Self-reported diagnosis of a Long-Term Condition

  • UK resident

  • Possession of an email address to enable all study procedures

  • Sufficient command of written and spoken English to understand study procedures

Exclusion Criteria:
  • Under the age of 18

  • Not living in the UK

  • No self-reported diagnosis of an LTC

  • Inability to complete questionnaires in English

Contacts and Locations

Locations

Site City State Country Postal Code
1 King's College London London United Kingdom SE1 9RT

Sponsors and Collaborators

  • King's College London

Investigators

  • Principal Investigator: Rona Moss-Morris, PhD, King's College London
  • Study Director: Annie Jones, PhD, King's College London
  • Study Director: Emma Jenkinson, MSc, King's College London
  • Study Director: Natasha Seaton, MSc, King's College London

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
King's College London
ClinicalTrials.gov Identifier:
NCT06072287
Other Study ID Numbers:
  • HR/DP-22/23-36320
First Posted:
Oct 10, 2023
Last Update Posted:
Oct 12, 2023
Last Verified:
Sep 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by King's College London
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 12, 2023