OPEN Study: Pain Management Treatment Needs Interviews

Sponsor
King's College London (Other)
Overall Status
Completed
CT.gov ID
NCT02972606
Collaborator
Imperial College London (Other), Chelsea and Westminster NHS Foundation Trust (Other), University College, London (Other)
26
2
8.9
13
1.5

Study Details

Study Description

Brief Summary

Presently, there are few options for medically managing HIV-related painful peripheral sensory neuropathy (HIV-SN). Psychological treatments, including Cognitive Behavioural Therapy (CBT), represent a potentially viable addition to the treatment of painful HIV-SN. However, there is a scarcity of research on psychological treatment approaches for pain management in people with HIV. This study will use in-depth semi-structured interviews to examine the needs of people with painful HIV-SN for a psychologically-based pain management treatment that may be delivered over the Internet. Interview questions will examine participants' needs in terms of treatment content and delivery format. Men and women, ethnic minorities, and people who use recreational drugs will be sampled to ensure that interview responses reflect the views of people most commonly suffering from this condition. Approximately 30 people will be recruited for the study. The interviews will be audio recorded, transcribed verbatim, and coded to identify themes. The interview responses will be used to develop and tailor a version of CBT for people with painful HIV-SN. It is hoped that tailoring the treatment based on the qualitative interview responses will increase the acceptability of the treatment and will improve treatment adherence rates for a future study.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    This report is independent research supported by the National Institute for Health Research (NIHR Post Doctoral Fellowship, Dr Whitney Scott, PDF-2015-08-059). The views expressed in this publication are those of the authors and not necessarily those of the NHS, the National Institute for Health Research or the Department of Health.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    26 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Cross-Sectional
    Official Title:
    Online Psychological Treatment for People With Painful HIV-related Peripheral Neuropathy (OPEN Study): Qualitative Investigation of Treatment Needs
    Study Start Date :
    Nov 1, 2016
    Actual Primary Completion Date :
    Jul 31, 2017
    Actual Study Completion Date :
    Jul 31, 2017

    Outcome Measures

    Primary Outcome Measures

    1. Semi-structured Interview [Day 1]

      Semi-structured interview performed at one occasion where the patient describes his/her experience living with painful peripheral neuropathy and his/her thoughts about a psychological treatment for managing pain.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Adults aged 18 years or older.

    • Living with HIV.

    • A positive screen for peripheral sensory neuropathy, as indicated by: presence of self-reported bilateral foot pain and/or numbness in a symmetrical distribution.

    • Positive screen for symptoms of neuropathic pain in the feet, as indicated by a score of greater than or equal to 3 on the patient reported outcomes section of the Neuropathic Pain Interview.

    • Pain in the feet present most days for at least 3 months.

    • Average pain intensity of greater than or equal to 4/10.

    • Average interference of pain with daily activities is greater than or equal to 4/10.

    Exclusion Criteria:
    • Presence of excessive alcohol consumption, hypothyroidism, vitamin B12 deficiency, diabetes, exposure to isoniazid or chemotherapy drug treatment, or a known history of a neuropathy due to a cause other than HIV or antiretroviral treatment

    • Unable to conduct interview in English.

    • Current diagnosis of dementia or learning disability.

    • Unwilling to provide written informed consent.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 King's College London London United Kingdom SE1 9RT
    2 Chelsea & Westminster Hospital NHS Foundation Trust London United Kingdom SW10 9NH

    Sponsors and Collaborators

    • King's College London
    • Imperial College London
    • Chelsea and Westminster NHS Foundation Trust
    • University College, London

    Investigators

    • Principal Investigator: Whitney Scott, PhD, King's College London

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    King's College London
    ClinicalTrials.gov Identifier:
    NCT02972606
    Other Study ID Numbers:
    • 205949
    First Posted:
    Nov 23, 2016
    Last Update Posted:
    Sep 6, 2017
    Last Verified:
    Sep 1, 2016
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Keywords provided by King's College London
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 6, 2017