Effectiveness of a Digital Health Application for Multiple Sclerosis (Levidex)
Study Details
Study Description
Brief Summary
The trial aims to evaluate the effectiveness of a novel digital health application (levidex), which was designed to increase quality of life in persons with multiple sclerosis (MS). Therefore, 470 people with MS will be recruited and randomized to two groups: (1) an intervention group that will receive access to levidex in addition to treatment as usual (TAU) (n = 235) and (2) a control group receiving an overview of relevant brochures from the Deutsche Multiple Sklerose Gesellschaft (German Multiple Sclerosis Society) on the topic of lifestyle in MS in addition to TAU (n = 235).The primary outcome measure is the total score on the Hamburg Quality of Life Questionnaire for Multiple Sclerosis (HALEMS), collected 6 months post-randomization.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Intervention group Participants allocated to the intervention group will receive access to levidex in addition to treatment as usual (TAU). levidex is a digital health application designed for individuals with Multiple Sclerosis (MS), accessible through a web browser. The application comprises 16 modules, with the majority focusing on treatment methods derived from cognitive behavioral therapy (CBT) and health behavior change. The program operates through interactive "dialogues", which are accompanied by illustrations, audio recordings, motivating text messages, worksheets, and summaries. Users are also encouraged to regularly complete short questionnaires to monitor their complaints. Once registered, the program remains accessible for 365 days. |
Behavioral: levidex
Participants will receive access to the digital health application levidex in addition to treatment as usual (TAU).
Other: treatment as usual (TAU)
treatment as usual (TAU)
|
| Active Comparator: Control group Participants allocated to the control group will receive an overview of relevant brochures from the Deutsche Multiple Sklerose Gesellschaft (German Multiple Sclerosis Society) on the topic of lifestyle in Multiple Sclerosis (MS) in addition to treatment as usual (TAU). After 6 months, they will be offered access to levidex. |
Behavioral: Control
Participants will receive access to an overview of relevant brochures from the Deutsche Multiple Sklerose Gesellschaft (German Multiple Sclerosis Society) on the topic of lifestyle in MS in addition to treatment as usual (TAU).
Other: treatment as usual (TAU)
treatment as usual (TAU)
|
Outcome Measures
Primary Outcome Measures
- Hamburg Quality of Life Questionnaire for Multiple Sclerosis (HALEMS) [6 months after randomization]
The HALEMS measures MS-specific quality of life. It covers the following domains: fatigue, thinking, mobility lower limb, mobility upper limb, communication and mood. The total score is calculated as the average of the scores in the six domains and ranges from 1 to 5. Higher scores represent lower quality of life.
Secondary Outcome Measures
- Patient Health Questionnaire (PHQ-9) [3 and 6 months after randomization]
The PHQ-9 measures depressive symptoms. Each of the 9 items is answered on a 4-point Likert scale ranging from 0 (not at all) to 3 (almost every day). The total score ranges from 0 to 27. Higher scores represent higher depressive symptoms.
- Work and Social Assessment Scale (WSAS) [3 and 6 months after randomization]
The WSAS measures an individual's perception of work and social functioning. It consists of 5 items that are answered on a 9-point Likert scale ranging from 0 (not at all impaired) to 8 (very severely impaired). The total score has a range of 0-40, with higher scores representing higher disability.
- Global index score of the Multiple Sclerosis International Quality of Life (MuSiQoL) [3 and 6 months after randomization]
The MuSiQoL measures MS-specific quality of life. It comprises 31 items covering 9 domains (activities of daily living, psychological well-being, symptoms, relationships with friends, relationships with family, relationships with the healthcare system, sentimental and sexual life, coping, and rejection). Each item is scored on a 6-point Likert scale. The score on each dimension is obtained by computing the mean of the item scores for that dimension. All dimension scores are linearly transformed to a 0-100 scale. The global index score is computed as the mean of the dimension scores. Higher scores represent higher quality of life.
- Generalized Anxiety Disorder Scale-7 (GAD-7) [3 and 6 months after randomization]
The GAD-7 is a 7-item self-report anxiety questionnaire. Items are rated on a 4-point Likert scale ranging from 0 (not at all) to 3 (nearly every day). The total score can range from 0 to 21, higher scores representing higher anxiety.
- Frenchay Activities Index (FAI) [3 and 6 months after randomization]
The FAI assesses participation in social and lifestyle activities with 15 items that are scored on a 4-point Likert scale ranging from 1 to 4. It covers three subdomains (domestic chores, outdoor, work/leisure activities). The total score ranges from 15 to 60. Higher scores represent more activity.
- Hamburg Quality of Life Questionnaire for Multiple Sclerosis (HALEMS) [3 months after randomization]
The HALEMS measures MS-specific quality of life. It covers the following domains: fatigue, thinking, mobility lower limb, mobility upper limb, communication and mood. The total score is calculated as the average of the scores in the six domains and ranges from 1 to 5. Higher scores represent lower quality of life.
Other Outcome Measures
- HALEMS Subscales (cognition; fatigue; mobility lower limb; mobility upper limb; communication; and mood) [3 and 6 months after randomization]
The HALEMS measures MS-specific quality of life. It covers the following domains: fatigue, thinking, mobility lower limb, mobility upper limb, communication and mood. each domain score ranges from 1 to 5. Higher scores represent lower quality of life.
- Intake of disease-modifying drugs overall (last 3 months) [3 and 6 months after randomization]
- Intake of DMDs classified according to efficacy (category 1-3, according to current German clinical guideline) (last 3 months) [3 and 6 months after randomization]
- Number of days on sick leave/sick pay (last 3 months) [3 and 6 months after randomization]
- Number of days in inpatient treatment (last 3 months) [3 and 6 months after randomization]
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Age ≥ 18
-
Impaired health-related quality of life (total score of the Hamburg Quality of Life Questionnaire for Multiple Sclerosis [HALEMS] ≥ 2)
-
Specialist treatment in the last three months before study inclusion
-
Diagnosis of MS (relevant ICD-10-GM diagnoses G35.x), confirmed by a medical document or equivalent certificate
-
Sufficient cognitive and motor skills to use an online program
-
Consent to participate
-
Sufficient knowledge of the German language
-
Access to the Internet
Exclusion Criteria:
- Presence of severe impairment of independence or abilities (degree of care ["Pflegegrad", § 15 SGB XI] ≥ 3)
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | GAIA AG | Hamburg | Germany | 22085 |
Sponsors and Collaborators
- Gaia AG
- University Hospital Schleswig-Holstein
- Universität Duisburg-Essen
Investigators
- Principal Investigator: Kamila Jauch-Chara, MD, University Hospital Schleswig-Holstein
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- levidex RCT 2023