- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02777944
Motivate: A Web-based Intervention
Motivate: A Web Based Intervention to Increase Attendance at an Eating Disorder Service
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
MotivATE is a web-based intervention intended to be delivered at the point of referral to an Eating Disorder (ED) service. The intervention focuses on managing expectations of assessment, addressing ambivalence and increasing users' motivation and confidence to attend their initial appointment. This is achieved through the use of information, motivational tools, interactive activities and stories from other individuals with EDs spread across four 15-20 minute modules. These modules have been evaluated by service-users who have an ED.
The aim of this study is to test whether MotivATE can increase attendance at assessment. This will be done using a single-consent Zelen randomised control trial, with all non-emergency adult clients referred to the Kimmeridge Courte Eating Disorder Service over a one year period being randomised to either treatment as usual (TAU) or TAU plus access to the MotivATE intervention prior to their assessment appointment.
Routine audit data will be collected to compare the number of people who attend their assessment appointment in the MotivATE group verses the control group. Usage data generated by the intervention will also be assessed. Twenty participants from the MotivATE group will be invited to give qualitative feedback about their experience of the intervention.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion criteria
1) Referrals to the eating disorders service during the study period.
Exclusion criteria
- Inpatients or emergency and urgent cases.
- Patients who have already been randomised into the study.
- Non English speakers
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control
Usual Care
|
|
|
Experimental: Intervention
Access to Motivate: a web-based intervention, in addition to Usual Care
|
A web-based intervention focuses on managing expectations of assessment, addressing ambivalence and increasing users' motivation and confidence to attend their initial appointment.
This is achieved through the use of information, motivational tools, interactive activities and stories from other individuals with EDs spread across four 15-20 minute modules.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of Participants Who Attended Initial Assessment Appointment
Time Frame: 3 months
|
Attendance at initial assessment appointment
|
3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of Participants Who Accessed the Intervention Program
Time Frame: 3 months
|
Number of participants who accessed the intervention program
|
3 months
|
|
Number of Participants Who Volunteered to Provide Qualitative Feedback on the Motivate Program
Time Frame: 3 months
|
Number of participants who volunteered to provide qualitative feedback on the Motivate Program
|
3 months
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Director: Katherine M Appleton, PhD, Bournemouth University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- PhDDay
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Eating Disorders
-
Ibn Haldun UniversityCompletedDisordered Eating Behaviors | Eating Pathology | Eating Disorders SymptomsTurkey
-
Ibn Haldun UniversityActive, not recruitingDisordered Eating Behaviors | Eating Pathology | Eating Disorder SymptomsTurkey
-
University of PalermoUniversity of Padova; University of CatanzaroRecruitingEating Disorders | Eating Behavior | Eating Disorder SymptomItaly
-
Axsome Therapeutics, Inc.Enrolling by invitationBinge-Eating DisorderUnited States
-
BioprojetCompleted
-
Ali RezaiActive, not recruiting
-
Axsome Therapeutics, Inc.RecruitingBinge-Eating DisorderUnited States
-
Otsuka Pharmaceutical Development & Commercialization...CompletedBinge-Eating DisorderUnited States
-
Bezmialem Vakif UniversityMuğla Sıtkı Koçman University; The Scientific and Technological Research Council... and other collaboratorsActive, not recruitingEating Disorders | Eating Behavior | Orthodontic Appliance Complication | Eating HabitTurkey
-
University of North Carolina, Chapel HillThe Hilda & Preston Davis Foundation; Global Foundation for Eating DisordersCompletedEating Disorder | Binge-eating DisorderUnited States
Clinical Trials on Motivate: a web-based intervention
-
VA Office of Research and DevelopmentMichael E. DeBakey VA Medical Center; Dallas VA Medical CenterRecruitingDepression | Musculoskeletal Pain | Aging | Chronic Back PainUnited States
-
University of RwandaUniversity of Ibadan; University of Peradeniya; Saveetha University; Usmanu Danfodiyo...Not yet recruitingOral Cancer | Health Education, Community | Digital Intervention | MHealth Application | MHealth InterventionRwanda, India, Nigeria, Sri Lanka
-
Cardenal Herrera UniversityCompleted
-
Northwestern UniversityWithdrawnIndividuals at Risk for DepressionUnited States
-
NYU Langone HealthStanford University; Shaare Zedek Medical CenterCompletedAnxiety Disorders | Major Depression | Post Traumatic Stress DisorderIsrael
-
Taipei Medical UniversityRecruitingInfertility | Heart Rate Variability | BiofeedbackTaiwan
-
Taipei Medical UniversityRecruitingParenting | Psychological Distress | Self EfficacyTaiwan
-
Heidelberg UniversityCompetence Network for Congenital Heart DefectsCompletedCongenital Heart Disease | Emotional RegulationGermany
-
Milton S. Hershey Medical CenterNational Heart, Lung, and Blood Institute (NHLBI)CompletedHypertensionUnited States
-
Georgetown UniversityAlbert Einstein College of Medicine; University of MichiganCompletedTobacco Cessation | Tobacco Use Disorder | Tobacco Use Cessation | Tobacco Dependence | Virus, Human Immunodeficiency | Tobacco-Use DisorderUnited States