PHOENIX: Craving Management Smartphone Application

Sponsor
Centre Hospitalier St Anne (Other)
Overall Status
Recruiting
CT.gov ID
NCT06140472
Collaborator
Direction Générale de l'Offre de Soins (Other)
160
2
2
54.6
80
1.5

Study Details

Study Description

Brief Summary

The objective of this study is to evaluate the effectiveness of the addition of nursing follow-up and the PHOENIX application, a personalized and self-adaptive Smartphone application, on the management of craving in patients with addictive disorders followed on an outpatient basis.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Phoenix
  • Behavioral: Journal de bord
N/A

Detailed Description

Addictive disorders are a public health priority. The management of addictive disorders aims to reduce addictive behaviour or abstinence, implying that the patient can overcome the urge to engage in this behaviour, a symptom called craving.

Craving, as a major motivational substrate for addictive behaviour, is a preferred therapeutic target for the management of addictive disorders. However, to date, there are no fully effective drugs or psychological interventions. Smartphone applications seem to have an interest in this context, with many advantages: accessibility, anonymity, ease of access and low cost. Sainte Anne's Hospital Moreau de Tour facility (Paris, France) was one of the pioneering centres in the management of addictive disorders. The nursing team has developed expertise in this field. Patients report difficulties to nurses about managing their craving on their own, and ask for more frequent interviews or even daily support. During practice analysis meetings, caregivers sought innovative solutions to optimize this care. Our team has designed the PHOENIX application, which allows us to support patients in real time who wish to reduce or stop their addictive behaviours. Used between two consultations, it targets craving, without being specific to a product or addictive behaviour. When the patient has a craving, PHOENIX identifies the situation and proposes the most appropriate strategy to avoid using. Strategies are personalized and self-adaptive. The application allows caregivers to monitor patients' progress and progress.

Hypothesis of this study: The PHOENIX application used as a complement to nursing care will allow a better management of craving and a decrease in relapses compared to usual care (usual care: multidisciplinary care including nursing care).

Study Design

Study Type:
Interventional
Anticipated Enrollment :
160 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Effectiveness of the PHOENIX Smartphone Application on the Nursing Management of Craving in Patients With Addictive Disorders Followed on an Outpatient Basis
Actual Study Start Date :
Dec 11, 2019
Anticipated Primary Completion Date :
Dec 30, 2023
Anticipated Study Completion Date :
Jun 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Phoenix application

Specific individualized nurse follow-up using the PHOENIX application.

Behavioral: Phoenix
Specific individualized nurse follow-up using the PHOENIX application.

Sham Comparator: Journal de bord

Regular nursing follow-up, with the use of an electronic journal.

Behavioral: Journal de bord
Regular nursing follow-up, with the use of an electronic journal.

Outcome Measures

Primary Outcome Measures

  1. median craving intensity at 6 months [6 months visit]

    Measurement of craving intensity with an analog visual scale (AVS) between 0 (no craving) and 10 (maximum imaginable craving), informed during craving episodes by the patient via the PHOENIX application or the electronic journal. Over the last 30 days before the visit at 6 months

Secondary Outcome Measures

  1. Number of cravings [0,3,6 and 12 months visit]

    The cravings will be informed by the patient during craving episodes via the PHOENIX application or the electronic journal

  2. Daily frequency of cravings [0,3,6 and 12 months]

    The cravings will be informed by the patient during craving episodes via the PHOENIX application or the electronic journal

  3. Median of the intensity of the cravings [0, 3, and 12 months visit]

    Measurement of craving intensity with an analog visual scale (AVS) between 0 (no craving) and 10 (maximum imaginable craving), informed during craving episodes by the patient via the PHOENIX application or the electronic journal. Over the last 15 days before the visit at 0, 3 and 12 months

  4. Number of addictive behavioural episodes [0,3,6 and 12 months]

    Addictive behaviors will be informed via the phoenix application or the electronic journal

  5. Frequency of addictive behavioural episodes [0,3,6 and 12 months]

    Addictive behaviors will be informed via the phoenix application or the electronic journal

  6. Type of addictive behavioural episodes [0,3,6 and 12 months visit]

    Addictive behaviors will be informed via the phoenix application or the electronic journal

  7. Severity of addictive disorder: addictive substance disorder or pathological gambling [0,3,6 and 12 months]

    Severity of the disorder assessed by the number of diagnostic criteria for addictive substance disorder or pathological gambling on the Diagnostic and Statistical Manuel of mental disorders (DSM-5).

  8. Severity of addictive disorder: Yale Food Addiction Scale (YFAS) food addiction score for bulimia nervosa [0 and 12 months visit]

    Severity of the food addiction for bulimia nervosa is assessed by the Yale Food Addiction Scale (YFAS). The YFAS assesses addiction-like eating of palatable foods based on the 11 diagnostic criteria for substance use disorder in the Diagnostic and Statistical Manual of Mental Disorders (DSM-5). No Food Addiction = 0-1 symptoms/score; Mild Food Addiction = 2 or 3 symptom/score; Moderate Food Addiction = 4 or 5 symptom/score; Severe Food Addiction = 6 or higher symptom/score

  9. Severity of addictive disorder: sexual addiction (Carnes criteria) [0,3,6 and 12 months visit]

    Severity of the disorder assessed by the number of positive responses in the Carnes criteria. Carnes criteria consists of 25 yes/no questions. If the answer is "yes" to 13 or more questions, the patient can be diagnosed as a sex addict (range: 0-25).

  10. Impulsivity (UPPS scale) [0,3,6 and 12 months]

    Impulsivity is assessed using the UPPS scale (Urgency, Premeditation (lack of), Perseverance (lack of), Sensation seeking. The UPPS impulsivity scale is a 45-item self-questionnaire that measures impulsivity by exploring: urgency (12 items: range 12-48), lack of forethought (11 items; range:11-44), lack of perseverance (10 items; range:10-40) and sensation seeking (12 items; range:12-48). For each subdimension, a high score indicates a high level of impulsivity.

  11. Number of strategies to deal with craving according to the type of addictive behaviour [0,3,6 and 12 months]

    The strategies will be provided through the application or the electronic journal

  12. Multidimensional evaluation of coping (Brief Cope scale by Muller and Spitz) [0,3,6 and 12 months]

    The multidimensional evaluation of coping is carried out using the Brief Coping Orientation to Problems Experienced (Brief COPE) ,28-item self-questionnaire. The Brief COPE contains 28 statements and 14 scales, each consisting of 2 statements. It is a self-administered questionnaire. It is available in 2 formats: 1) dispositional, which is designed to assess how people habitually respond to stressful situations, and 2) situational, which is designed to assess how people responded to a specific event or context that has recently become a source of stress. Only the verb tense varies between statements in the two formats. The respondent uses a 4-point scale to give his/her answer to each statement: 1 - not at all; 2 - a little; 3 - a lot; 4 - completely. The answers obtained are added together for each scale. Higher scores on a scale indicate greater use of this coping mechanism.

  13. Anxiety: Beck's inventory for anxiety (BAI) [0,3,6 and 12 months]

    The anxiety assessment is carried out using Beck's inventory for anxiety (BAI). The Beck Anxiety Inventory (BAI) is a 21-question multiple-choice self-report inventory used to measure the severity of anxiety. The questions used in this measure ask to describe common symptoms of anxiety that the subject has experienced in the last week (including the day on which the measure is taken). The BAI contains 21 questions, each answer being scored on a scale value of 0 (not at all) to 3 (severely). Higher total scores indicate more severe anxiety symptoms. The standardized cutoffs are: 0-7: Minimal 8-15: Mild 16-25: Moderate 26-63: Severe

  14. Depression: Beck's depression inventory [0,3,6 and 12 months]

    The Beck Depression Inventory (BDI), is a multiple-choice self-report inventory for measuring the severity of depression. The BDI, consisted of twenty-one questions about how the subject has been feeling in the last week. Each question had a set of at least four possible responses, ranging in intensity: (0) I do not feel sad I feel sad. I am sad all the time, and I cannot snap out of it. I am so sad or unhappy that I cannot stand it. When the test is scored, a value of 0 to 3 is assigned for each answer, and then the total score determines the depression's severity. The standard cut-off scores were as follows: 0-9: indicates minimal depression 10-18: indicates mild depression 19-29: indicates moderate depression 30-63: indicates severe depression. Higher total scores indicate more severe depressive symptoms.

  15. Quality of life: World Health Organization Quality of Life (WHOQOL 26 scale) [0,3,6 and 12 months]

    The World Health Organization Quality of Life (WHOQOL26) assesses subjective health-related quality of life in a 26-item self-administered questionnaire. The WHOQOL26 scale investigates the quality of life in four domains: physical health (7 items), psychological health (6 items), social relationships (3 items) and environmental health (8 items); it also contains QOL and general health items. Each item of the WHOQOL26 is scored on a five-point ordinal scale. The scores are then linearly transformed into a 0-100 scale.

  16. Self-esteem (Coopersmith inventory) [0,3,6 and 12 months]

    The Coopersmith's Self-Esteem Inventory assesses general, professional, social and family self-esteem; the total is the sum of these four components. The test comprises 58 items; the responses are "looks like me" or "doesn't look like me." The score is composed of several subscales: General (26 items), Social (8 items), Professional (8 items), Family (8 items) and Lie (8 items). The total score (50 items) is obtained by summing the General, Social, Professional and Family subscales. The Lying scale is more of a social desirability scale used to assess patient authenticity in general assessment.

  17. Use of healthcare related to addictive disorder: Hospitalisation [0,3,6 and 12 months]

    Number of hospitalization days related to addiction

  18. Use of healthcare related to addictive disorder: emergency department accesses [0,3,6 and 12 months]

    Number of emergency department accesses related to addiction

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Being 18 and 65 years old, any sex

  • Speak and read French

  • Have a Smartphone (Android operating system or IOS)

  • Present an evaluated addictive disorder in a structured clinical interview (MINI, adapted to the criteria of DSM-5: substance use disorder according to DSM-5 and bulimia nervosa; National Opinion DSM Screen (NODS), adapted to the criteria of DSM-5: pathological gambling; NODS, adapted to the diagnostic criteria proposed by Carnes: sexual addiction ; MINI)

  • Be followed on an outpatient basis

  • Prior informed written consent of the patient or his or her legal representative

  • Benefit from a French social protection system

Exclusion Criteria:
  • Have a current untreated and/or unstabilized psychiatric disorder (assessed by MINI)

  • Have a severe cognitive impairment assessed during the clinical interview, which does not allow you to focus your attention or use the working memory required by the application.

  • Pregnant or breastfeeding women

  • Participant in another clinical trial

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hospices Civiles de Lyon Lyon France
2 CHU de Nantes Nantes France

Sponsors and Collaborators

  • Centre Hospitalier St Anne
  • Direction Générale de l'Offre de Soins

Investigators

  • Principal Investigator: Chloe Lucet, PH, Centre Hospitalier St Anne

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centre Hospitalier St Anne
ClinicalTrials.gov Identifier:
NCT06140472
Other Study ID Numbers:
  • D19-P019
First Posted:
Nov 20, 2023
Last Update Posted:
Nov 20, 2023
Last Verified:
Nov 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Centre Hospitalier St Anne

Study Results

No Results Posted as of Nov 20, 2023