Effectiveness of a Digital Health Application for Subacute and Chronic Back Pain (Relevis)

NCT06221956 | Recruiting

• 1 other identifier: relevis RCT 2024
• Study Type: interventional
• Target: 276
• Locations: 1 country
• Sites: 1

Brief Summary

This clinical trial with 276 patients with subacute or chronic back pain aims to investigate the effectiveness of the unguided digital therapeutic relevis for patients with subacute or chronic back pain. Inclusion criteria are: age ≥ 18 years, presence of subacute (6-12 weeks) or chronic (\>12 weeks) back pain, attested by a medical certificate (relevant ICD-10-GM diagnoses: M47.8x, M47.9x, M54.5, M54.8x, M54.9x, M51.0x, M51.1x, M51.2), impaired functional ability \[Oswestry Disability Index (ODI) ≥ 21\], consent to participation, sufficient knowledge of the German language. Exclusion criteria are: change in treatment of back pain in the past month, planned change in treatment of back pain in the next 3 months, prior use of other online programs/apps for back pain, history of back, hip or knee surgery in the past 6 months, history of more than one back surgery in lifetime, presence of a specific cause for back pain (e.g., fracture, infection, neuropathies \[except when due to disc prolapse\], axial spondyloarthritis), tumor or metastases, cauda equina syndrome, acute myocardial infarction, unstable coronary heart disease/angina pectoris or heart failure, acute thrombosis, manifest osteoporosis, acute fevers, rheumatic autoimmune diseases. Patients will be randomized and allocated to either an intervention group in a 1:1 ratio, in which they will receive access to relevis in addition to treatment as usual (TAU, n = 138), or to a control group, in which they will receive only TAU (n = 138). TAU is defined as any therapy prescribed or recommended by the GP or specialists (e. g. orthopedic surgeon, rheumatologists etc.) which may include physiotherapy, injections in the spine, drug therapy, orthesis, etc. (1,2). The primary endpoint will be the functional impairment, measured by the ODI, with three months post-allocation being the primary time point for assessment of effectiveness (T1). Six months post-allocation (T2) will be used as the follow-up assessment endpoint. Secondary endpoints will be depression, work and social functioning, pain intensity, and health-related quality of life.

Conditions

Back Pain

Outcome Measures

Primary Outcomes (1)

• Functional Impairment

  Oswestry Low Back Pain Disability Questionnaire (ODI). Total score ranging from 0-100; higher scores mean higher functional impairment (worse outcome).

  3 months

Secondary Outcomes (4)

• Depressive Symptomatology

  3 months

• Work and Social Functioning

  3 months

• Intensity of Back Pain

  3 months

• Health-related Quality of Life

  3 months

Study Arms (2)

relevis + TAU

EXPERIMENTAL

Participants allocated to the intervention group will receive access to relevis in addition to treatment as usual (TAU). relevis is a digital health application designed for individuals with subacute or chronic back pain, accessible through a web browser. The application consists of six physical exercise modules that cover four exercises with thiree different levels of difficulty, each, and ten interactive "conversations" on different topics (changes in the body, pain development and processing, chronic pain, pain and mood, relaxation and mindfulness, becoming active against pain, stress and pain, nutrition and pain, sleep and pain, work and pain). "Conversations" are accompanied by illsutrations, 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 180 days.

Behavioral: relevis

TAU

NO INTERVENTION

Participants allocated to the control group will receive access to treatment as usual (TAU).

Interventions

relevis BEHAVIORAL

Participants will receive access to the digital health intervention relevis in addition to TAU.

relevis + TAU

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Age ≥ 18
• Presence of subacute (6-12 weeks) or chronic (\>12 weeks) back pain
• Submission of a medical certificate attesting to the presence of at least one of the following ICD-10-GM diagnoses of back pain:
• M47.8x - Spondylosis
• M47.9x - Other spondylosis
• M54.5 - Back pain
• M54.8x - Other back pain
• M54.9x - Unspecified back pain
• M51.0x - Thoracic, thoracolumbar and lumbosacral intervertebral disc disorders with myelopathy
• M51.1x - Thoracic, thoracolumbar and lumbosacral intervertebral disc disorders with radiculopathy
• M51.2 - Other thoracic, thoracolumbar and lumbosacral intervertebral disc displacement
• Impaired functional ability (ODI ≥ 21)
• Consent to participate
• Sufficient knowledge of the German language

You may not qualify if:

• Change in treatment of back pain in the past month
• Planned change in treatment of back pain in the next 3 months
• Prior use of other online programs/apps for back pain
• History of back, knee or hip surgery in the past 6 months
• History of more than one back surgery during lifetime
• Presence of a specific cause for back pain, e.g.:
• Fracture
• Infection
• Neuropathies (except when due to disc prolapse)
• Axial spondyloarthritis
• Tumor or metastases
• Cauda equina syndrome
• Acute myocardial infarction
• Unstable coronary heart disease/angina pectoris or heart failure
• Acute thrombosis

Sponsors & Collaborators

• Gaia AG: lead
• University Hospital Schleswig-Holstein: collaborator
• Philipps Universität Marburg: collaborator

Study Sites (1)

GAIA AG

Hamburg, 22085, Germany

RECRUITING

MeSH Terms

Conditions

Back Pain

Condition Hierarchy (Ancestors)

Pain; Neurologic Manifestations; Signs and Symptoms; Pathological Conditions, Signs and Symptoms

Study Officials

• Kamila Jauch-Chara, MD

  University Hospital Schleswig-Holstein

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Gitta A. Jacob, PhD

CONTACT

+49.40.349930-374; gitta.jacob@gaia-group.com

Antje Riepenhausen, PhD

CONTACT

antje.riepenhausen@gaia-group.com

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: January 15, 2024
• First Posted: January 24, 2024
• Study Start: January 23, 2024
• Primary Completion: January 23, 2025
• Study Completion: January 23, 2025
• Last Updated: February 9, 2024

Record last verified: 2024-02

Data Sharing

• IPD Sharing: Will not share

Locations

DE (1)