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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03275649
Other study ID # CityULondon_PDHelp
Secondary ID
Status Completed
Phase N/A
First received August 29, 2017
Last updated January 29, 2018
Start date July 21, 2017
Est. completion date January 1, 2018

Study information

Verified date January 2018
Source City, University of London
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Non-motor symptoms (NMS) are common in Parkinson's disease (PD) and cause significant distress and decreased quality of life. A high rate of non-declaration of NMS by patients means that many NMS remain unrecognized and untreated, even in specialist clinical services. In phase one of this research qualitative interviews (phase 1) were guided by the Theoretical Domains Framework and used to identify the barriers for help-seeking. A quantitative questionnaire survey (phase 2) examined the significance of these barriers to help seeking. The present study aims to develop (phase 3) and test the feasibility (phase 4) of a targeted behavioural intervention of barriers which were identified in phases 1 and 2 which prevent help-seeking for NMS in patients with PD. As with phases 1 and 2, the feasibility trial will include people with unreported burdensome NMS, who have not reported them to their PD consultant or nurse. The intervention has been co-designed by people affected by Parkinson's and targets the barriers identified in the previous phases of the research. In phase three of the research, 'think-aloud' interviews will be used to further develop the intervention so that it is acceptable and easy to use. In the final phase, a feasibility trial will be conducted to examine efficacy of the intervention for increasing help-seeking for undeclared NMS. The study has implications for using a theoretically driven behavioural intervention to promote help-seeking for NMS and ultimately increase receipt of clinical care for NMS among patients with PD.


Recruitment information / eligibility

Status Completed
Enrollment 35
Est. completion date January 1, 2018
Est. primary completion date January 1, 2018
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Diagnosis of idiopathic Parkinson's

- Access to a computer and internet connection

- Experiencing at least one unreported non-motor symptom

Exclusion Criteria:

- Presence of sensory loss or communication difficulty (including inadequate command of English) sufficient to interfere with the assessments.

- Severe cognitive impairment that would make participation in the intervention problematic or distressing. This will be assessed using the Telephone Interview for Cognitive Status-Modified (TICS-M, Brandt et al., 1993). People with a score of less than 20 will be excluded.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Help-seeking for non-motor symptoms
Brief, self-paced, online individually tailored intervention using LifeGuide software. Includes information, videos and exercises.

Locations

Country Name City State
United Kingdom City, University of London London

Sponsors (3)

Lead Sponsor Collaborator
City, University of London King's College Hospital NHS Trust, King's College London

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Proportion of patients help-seeking post-intervention after intervention 1 week
Secondary Number of eligible patients completing the study 1 week
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