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Prevention of Comorbid Depression and Obesity in Attention-deficit/ Hyperactivity Disorder (PROUD)

Primary Purpose

Attention-Deficit / Hyperactivity Disorder, Depression, Obesity

Status
Completed
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
Bright light therapy
Physical exercise
Sponsored by
Goethe University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Attention-Deficit / Hyperactivity Disorder focused on measuring attention-deficit / hyperactivity disorder, depression, obesity, prevention, bright light therapy, exercise, mobile healthy system

Eligibility Criteria

14 Years - 45 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of ADHD according to Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) criteria
  • Stable treatment as usual comprising pharmacotherapy, group based or individual cognitive behavioural therapy (not including elements of bright light therapy or exercise)

Exclusion Criteria:

  • Intelligence Quotient (IQ) below 75
  • Any severe (comorbid) psychiatric disorder with necessary additional psychopharmaco or daycare/ inpatient therapy beyond treatment as usual
  • Severe medical/ neurological condition not allowing bright light therapy or exercise
  • History of epilepsy
  • Use of antipsychotics, antiepileptic or photosensitising medication
  • Substance abuse/ dependency

Sites / Locations

  • Goethe University Hospital Frankfurt, Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, and Department of Psychiatry, Psychosomatic Medicine and Psychotherapy
  • Radboud University Medical Centre, Karakter Child and Adolescent Psychiatry, and Department of Psychiatry
  • Vall d'Hebron Research Institute, Group of Psychiatry, Mental Health and Addiction
  • King's College London, Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

No Intervention

Arm Label

Bright light therapy

Physical exercise

Treatment as usual

Arm Description

Mobile therapeutic light (10.000 LUX), daily (except Sunday) for 30 min in the morning or evening for 10 weeks in total. Additional treatment as usual comprising pharmacotherapy, group based or individual cognitive behavioural therapy (not including elements of bright light therapy or exercise) is allowed.

Aerobic exercise of moderate-to-vigorous intensity three days a week plus muscle-strengthening exercises two days a week during 10 weeks in total. Additional treatment as usual comprising pharmacotherapy, group based or individual cognitive behavioural therapy (not including elements of bright light therapy or exercise) is allowed.

Stable treatment as usual comprising pharmacotherapy, group based or individual cognitive behavioural therapy (not including elements of bright light therapy or exercise).

Outcomes

Primary Outcome Measures

Change from baseline in clinician-rated depressive symptoms (observer-blinded assessment)
Inventory of Depressive Symptomatology (clinician-rated)

Secondary Outcome Measures

Change from baseline in clinician-rated depressive symptoms (observer-blinded assessment)
Inventory of Depressive Symptomatology (clinician-rated)
Change from baseline in clinician-rated ADHD symptoms
ADHD Rating Scales for adults and children
Change from baseline in self-reported severity of depressive symptoms
Beck Depression Inventory II
Change from baseline in self-reported health status
Health Questionnaire EQ-5D-3L
Change from baseline in self-reported health related quality of life
Short Form Health Questionnaire General Health Questionnaire
Change from baseline in self-reported general health status
General Health Questionnaire General Health Questionnaire
Change from baseline in self-reported emotional and behavioural problems in adolescents
Youth self-report
Change from baseline in self-reported emotional and behavioural problems in adults
Adult self-report
Change from baseline in circadian rhythm
Munich Chronotype Questionnaire
Change from baseline in cognitive emotion regulation
Cognitive Emotion Regulation Questionnaire
Change from baseline in neurocognitive functions: verbal memory
Rey Auditory Verbal Learning Test
Change from baseline in neurocognitive functions: Digit span
Digit span
Change from baseline in self-reported physical fitness
International Fitness Scale
Change from baseline in general muscular fitness
handgrip strength test
Change from baseline in muscular fitness
standing long jump test
Change from baseline in aerobic fitness
Chester step test
Change from baseline in body mass index
body mass index measured by clinician
Change from baseline in waist circumference
waist circumference measured by clinician
Change from baseline in waist-to-hip ratio
waist-to-hip ratio measured by clinician
Change from baseline in body fat percentage
based on skinfold thickness measurements using a skinfold caliper
Change from baseline in heart rate
heart rate measured by clinician
Change from baseline in blood pressure
blood pressure measured by clinician
Change from baseline in number of steps
number of steps measured with the mobile Health app
Change from baseline in movement acceleration
movement acceleration measured with the mobile Health app
Change from baseline in sleep time
sleep time measured with the mobile Health app
Change from baseline in context parameters
context measured with the mobile Health
Change from baseline in mood regulation
mood regulation measured with the mobile Health app
Change from baseline in reward reactivity
reward reactivity measured with the mobile Health app
Change from baseline in stress reactivity
stress reactivity measured with the mobile Health app
Change from baseline in inattention
inattention measured with the mobile Health app
Change from baseline in melatonin concentration
Saliva sample will be taken to measure melatonin concentration
Change from baseline in cortisol concentration
Saliva sample will be taken to measure cortisol concentration
Change from baseline in leptin concentration
Saliva sample will be taken to measure leptin concentration
Change from baseline in ghrelin concentration
Saliva sample will be taken to measure ghrelin concentration
Change from baseline in neural activity associated with reward processing
Striatal functional magnetic resonance imaging signal related to reward processing

Full Information

First Posted
March 3, 2017
Last Updated
October 14, 2020
Sponsor
Goethe University
Collaborators
Heidelberg University, Radboud University Medical Center, Hospital Vall d'Hebron, King's College London
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1. Study Identification

Unique Protocol Identification Number
NCT03371810
Brief Title
Prevention of Comorbid Depression and Obesity in Attention-deficit/ Hyperactivity Disorder
Acronym
PROUD
Official Title
Pilot Randomized-controlled Phase-IIa Trial on the Prevention of Comorbid Depression and Obesity in Attention-deficit/ Hyperactivity Disorder
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Completed
Study Start Date
March 13, 2017 (Actual)
Primary Completion Date
August 31, 2020 (Actual)
Study Completion Date
August 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Goethe University
Collaborators
Heidelberg University, Radboud University Medical Center, Hospital Vall d'Hebron, King's College London

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Depression and obesity are very common among adolescents and young adults with attention-deficit/ hyperactivity disorder (ADHD). However, intervention programmes to prevent these comorbid disorders rarely exist. In a pilot randomized-controlled study we test two newly developed intervention programmes that do not involve medication: bright light therapy and physical exercise. Both interventions will be supported by a mobile Health application to monitor and feedback intervention success and booster patients' motivation.
Detailed Description
The risk for comorbid major depressive disorder and obesity is increased in adolescents and adults with attention-deficit/ hyperactivity disorder (ADHD), and adolescent ADHD predicts adults major depressive disorder and obesity. Nonpharmacological interventions to prevent these comorbidities are urgently needed. Bright light therapy (BLT) improves day-night rhythm and is an established therapy for major depression in adolescents and adults. Exercise prevents and reduces obesity in adolescents and adults and also improves depressive symptoms. Interestingly, a reinforcement-based intervention using a mobile health app (m-Health) resulted in improved effects on weightloss in obesity. The aim of the current pilot randomized-controlled phase-IIa study is to establish feasibility and effect sizes of two kinds of interventions, BLT and exercise, in combination with m-Health based monitoring and reinforcement in adolescents and young adults aged 14 to 45 years old with ADHD, targeting the prevention of depressive symptoms and obesity. In addition, immediate and long-term treatment effects on ADHD specific psychopathology, health related quality of life, fitness and body related measures, neurocognitive functions and chronotype are explored. Furthermore, saliva samples are taken in a subgroup of adult patients to explore the effects of BLT and exercise on concentrations of hormones. This subgroup of adult patients will also participate in an additional neuroimaging study of the reward system in order to explore intervention effects on striatal reward reactivity.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Attention-Deficit / Hyperactivity Disorder, Depression, Obesity
Keywords
attention-deficit / hyperactivity disorder, depression, obesity, prevention, bright light therapy, exercise, mobile healthy system

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
Prospective, randomized, observer-blinded, controlled, multi-centre, pilot phase-IIa parallel-group design with three arms (two treatment groups and one control group); three trial phases: baseline assessment, 10 weeks of treatment versus treatment as usual; 12 weeks post-treatment observation period.
Masking
Outcomes Assessor
Masking Description
Observer-blinded assessment of the primary outcome measure
Allocation
Randomized
Enrollment
207 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Bright light therapy
Arm Type
Experimental
Arm Description
Mobile therapeutic light (10.000 LUX), daily (except Sunday) for 30 min in the morning or evening for 10 weeks in total. Additional treatment as usual comprising pharmacotherapy, group based or individual cognitive behavioural therapy (not including elements of bright light therapy or exercise) is allowed.
Arm Title
Physical exercise
Arm Type
Experimental
Arm Description
Aerobic exercise of moderate-to-vigorous intensity three days a week plus muscle-strengthening exercises two days a week during 10 weeks in total. Additional treatment as usual comprising pharmacotherapy, group based or individual cognitive behavioural therapy (not including elements of bright light therapy or exercise) is allowed.
Arm Title
Treatment as usual
Arm Type
No Intervention
Arm Description
Stable treatment as usual comprising pharmacotherapy, group based or individual cognitive behavioural therapy (not including elements of bright light therapy or exercise).
Intervention Type
Behavioral
Intervention Name(s)
Bright light therapy
Other Intervention Name(s)
Device: smartphone with m-Health app, Device: Philips EnergyLight HF 3419
Intervention Description
Mobile therapeutic light (10.000 LUX, white light without UV light), daily (except Sunday) for 30 min in the morning or evening for 10 weeks in total at home provided by a bright light therapy device (Philips EnergyLight HF 3419). Monitoring and feedback will be realized with the m-Health system comprising of a smartphone equipped with the m-Health App, and an activity sensor equipped with a light sensor to monitor the light exposure of the participant.
Intervention Type
Behavioral
Intervention Name(s)
Physical exercise
Other Intervention Name(s)
Device: smartphone with m-Health app
Intervention Description
During 10 weeks participants perform three days of aerobic activities proposed and in two of these days also do muscle-strengthening exercise. Specifically, a training day consists of: (i) a 5-min warm-up period, (ii) a 10-35 min of muscle-strength training on two of the three days, (iii) a 20-40 min of aerobic training, (iii), and a 5-min of flexibility/stretching cool-down. During the course of the 10 weeks, the duration and intensity of the exercises will increase gradually. Instruction, monitoring, and feedback will be realised by the m-Health system including a smartphone equipped with the m-Health app and Secure Digital Memory cards to store the exercise videos as well as an activity sensor equipped with a mobile sensor for the acquisition of physical activity.
Primary Outcome Measure Information:
Title
Change from baseline in clinician-rated depressive symptoms (observer-blinded assessment)
Description
Inventory of Depressive Symptomatology (clinician-rated)
Time Frame
baseline, end of intervention (10 weeks after baseline)
Secondary Outcome Measure Information:
Title
Change from baseline in clinician-rated depressive symptoms (observer-blinded assessment)
Description
Inventory of Depressive Symptomatology (clinician-rated)
Time Frame
baseline, follow up (22 weeks after baseline)
Title
Change from baseline in clinician-rated ADHD symptoms
Description
ADHD Rating Scales for adults and children
Time Frame
baseline, end of intervention (10 weeks after baseline), follow-up (22 weeks after baseline)
Title
Change from baseline in self-reported severity of depressive symptoms
Description
Beck Depression Inventory II
Time Frame
baseline, end of intervention (10 weeks after baseline), follow-up (22 weeks after baseline)
Title
Change from baseline in self-reported health status
Description
Health Questionnaire EQ-5D-3L
Time Frame
baseline, end of intervention (10 weeks after baseline), follow-up (22 weeks after baseline)
Title
Change from baseline in self-reported health related quality of life
Description
Short Form Health Questionnaire General Health Questionnaire
Time Frame
baseline, end of intervention (10 weeks after baseline)
Title
Change from baseline in self-reported general health status
Description
General Health Questionnaire General Health Questionnaire
Time Frame
baseline, end of intervention (10 weeks after baseline)
Title
Change from baseline in self-reported emotional and behavioural problems in adolescents
Description
Youth self-report
Time Frame
baseline, end of intervention (10 weeks after baseline), follow-up (22 weeks after baseline)
Title
Change from baseline in self-reported emotional and behavioural problems in adults
Description
Adult self-report
Time Frame
baseline, end of intervention (10 weeks after baseline), follow-up (22 weeks after baseline)
Title
Change from baseline in circadian rhythm
Description
Munich Chronotype Questionnaire
Time Frame
baseline, end of intervention (10 weeks after baseline), follow-up (22 weeks after baseline)
Title
Change from baseline in cognitive emotion regulation
Description
Cognitive Emotion Regulation Questionnaire
Time Frame
baseline, end of intervention (10 weeks after baseline), follow-up (22 weeks after baseline)
Title
Change from baseline in neurocognitive functions: verbal memory
Description
Rey Auditory Verbal Learning Test
Time Frame
baseline, end of intervention (10 weeks after baseline), follow-up (22 weeks after baseline)
Title
Change from baseline in neurocognitive functions: Digit span
Description
Digit span
Time Frame
baseline, end of intervention (10 weeks after baseline), follow-up (22 weeks after baseline)
Title
Change from baseline in self-reported physical fitness
Description
International Fitness Scale
Time Frame
baseline, end of intervention (10 weeks after baseline), follow-up (22 weeks after baseline)
Title
Change from baseline in general muscular fitness
Description
handgrip strength test
Time Frame
baseline, end of intervention (10 weeks after baseline), follow-up (22 weeks after baseline)
Title
Change from baseline in muscular fitness
Description
standing long jump test
Time Frame
baseline, end of intervention (10 weeks after baseline), follow-up (22 weeks after baseline)
Title
Change from baseline in aerobic fitness
Description
Chester step test
Time Frame
baseline, end of intervention (10 weeks after baseline), follow-up (22 weeks after baseline)
Title
Change from baseline in body mass index
Description
body mass index measured by clinician
Time Frame
baseline, end of intervention (10 weeks after baseline), follow-up (22 weeks after baseline)
Title
Change from baseline in waist circumference
Description
waist circumference measured by clinician
Time Frame
baseline, end of intervention (10 weeks after baseline), follow-up (22 weeks after baseline)
Title
Change from baseline in waist-to-hip ratio
Description
waist-to-hip ratio measured by clinician
Time Frame
baseline, end of intervention (10 weeks after baseline), follow-up (22 weeks after baseline)
Title
Change from baseline in body fat percentage
Description
based on skinfold thickness measurements using a skinfold caliper
Time Frame
baseline, end of intervention (10 weeks after baseline), follow-up (22 weeks after baseline)
Title
Change from baseline in heart rate
Description
heart rate measured by clinician
Time Frame
baseline, end of intervention (10 weeks after baseline), follow-up (22 weeks after baseline)
Title
Change from baseline in blood pressure
Description
blood pressure measured by clinician
Time Frame
baseline, end of intervention (10 weeks after baseline), follow-up (22 weeks after baseline)
Title
Change from baseline in number of steps
Description
number of steps measured with the mobile Health app
Time Frame
baseline, end of intervention (10 weeks after baseline)
Title
Change from baseline in movement acceleration
Description
movement acceleration measured with the mobile Health app
Time Frame
baseline, end of intervention (10 weeks after baseline)
Title
Change from baseline in sleep time
Description
sleep time measured with the mobile Health app
Time Frame
baseline, end of intervention (10 weeks after baseline)
Title
Change from baseline in context parameters
Description
context measured with the mobile Health
Time Frame
baseline, end of intervention (10 weeks after baseline)
Title
Change from baseline in mood regulation
Description
mood regulation measured with the mobile Health app
Time Frame
baseline, end of intervention (10 weeks after baseline)
Title
Change from baseline in reward reactivity
Description
reward reactivity measured with the mobile Health app
Time Frame
baseline, end of intervention (10 weeks after baseline)
Title
Change from baseline in stress reactivity
Description
stress reactivity measured with the mobile Health app
Time Frame
baseline, end of intervention (10 weeks after baseline)
Title
Change from baseline in inattention
Description
inattention measured with the mobile Health app
Time Frame
baseline, end of intervention (10 weeks after baseline)
Title
Change from baseline in melatonin concentration
Description
Saliva sample will be taken to measure melatonin concentration
Time Frame
baseline, end of intervention (10 weeks after baseline)
Title
Change from baseline in cortisol concentration
Description
Saliva sample will be taken to measure cortisol concentration
Time Frame
baseline, end of intervention (10 weeks after baseline)
Title
Change from baseline in leptin concentration
Description
Saliva sample will be taken to measure leptin concentration
Time Frame
baseline, end of intervention (10 weeks after baseline)
Title
Change from baseline in ghrelin concentration
Description
Saliva sample will be taken to measure ghrelin concentration
Time Frame
baseline, end of intervention (10 weeks after baseline)
Title
Change from baseline in neural activity associated with reward processing
Description
Striatal functional magnetic resonance imaging signal related to reward processing
Time Frame
baseline, end of intervention (10 weeks after baseline)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
14 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of ADHD according to Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) criteria Stable treatment as usual comprising pharmacotherapy, group based or individual cognitive behavioural therapy (not including elements of bright light therapy or exercise) Exclusion Criteria: Intelligence Quotient (IQ) below 75 Any severe (comorbid) psychiatric disorder with necessary additional psychopharmaco or daycare/ inpatient therapy beyond treatment as usual Severe medical/ neurological condition not allowing bright light therapy or exercise History of epilepsy Use of antipsychotics, antiepileptic or photosensitising medication Substance abuse/ dependency
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christine M Freitag, Prof. Dr.
Organizational Affiliation
Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital, Goethe University Frankfurt am Main
Official's Role
Principal Investigator
Facility Information:
Facility Name
Goethe University Hospital Frankfurt, Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, and Department of Psychiatry, Psychosomatic Medicine and Psychotherapy
City
Frankfurt am Main
Country
Germany
Facility Name
Radboud University Medical Centre, Karakter Child and Adolescent Psychiatry, and Department of Psychiatry
City
Nijmegen
Country
Netherlands
Facility Name
Vall d'Hebron Research Institute, Group of Psychiatry, Mental Health and Addiction
City
Barcelona
Country
Spain
Facility Name
King's College London, Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience
City
London
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
29482662
Citation
Mayer JS, Hees K, Medda J, Grimm O, Asherson P, Bellina M, Colla M, Ibanez P, Koch E, Martinez-Nicolas A, Muntaner-Mas A, Rommel A, Rommelse N, de Ruiter S, Ebner-Priemer UW, Kieser M, Ortega FB, Thome J, Buitelaar JK, Kuntsi J, Ramos-Quiroga JA, Reif A, Freitag CM. Bright light therapy versus physical exercise to prevent co-morbid depression and obesity in adolescents and young adults with attention-deficit / hyperactivity disorder: study protocol for a randomized controlled trial. Trials. 2018 Feb 26;19(1):140. doi: 10.1186/s13063-017-2426-1.
Results Reference
derived
Links:
URL
http://coca-project.eu/coca-phase-iia-trial/study/
Description
Homepage of the CoCA project (Comorbid Conditions of Attention-deficit / hyperactivity disorder).The PROUD study is work package 6 of the CoCA project.

Learn more about this trial

Prevention of Comorbid Depression and Obesity in Attention-deficit/ Hyperactivity Disorder

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