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Neurofeedback Training for the Treatment of Substance Use Disorders

S

Sorlandet Hospital HF

Status

Completed

Conditions

Substance Use Disorders

Treatments

Behavioral: Neurofeedback

Study type

Interventional

Funder types

Other

Identifiers

NCT03356210
SSHF_2017

Details and patient eligibility

About

The proposed randomized controlled trial (RCT) will investigate the usefulness of electroencephalographic (EEG) biofeedback, also called neurofeedback (NF), a treatment method that can potentially prevent relapses among patients with a substance use disorder (SUD) through its calming effect on the central nervous system.

The study will examine whether NF can improve general well-being and quality of life (QoL) and subsequently its ability to play a role in relapse prevention strategies. Specifically, the effect on physical and psychological distress will be investigated.

Full description

A patient with a substance use disorder (SUD) typically requires comprehensive and individualized care across different levels of service providers, from primary care to the specialist health care services. Among the known threats to a prolonged remission are negative emotional states because they can trigger the urge to use drugs. An integrative approach is warranted aimed to address the physiological, psychological and social aspects of the disorder during the rehabilitation period.

Patients with a SUD diagnosis in an outpatient clinic will be randomized to either 1) 20 sessions of symptom-based NF training in conjunction with traditional therapy or 2) conventional counseling. The primary outcome is QoL at the end of treatment and at a 3 and 12 month follow-up. Secondary outcome measures include alcohol and drug use, mental distress, sleep quality and cognitive function. The optimal quantity of the intervention will be assessed with a cost-benefit approach.

The proposed study will provide new knowledge about how NF can be best utilized in SUD treatment, potentially improving QoL and relapse rates.

Enrollment

93 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with a substance use disorder referred to outpatient addiction treatment, aged >18 of both genders.

Exclusion criteria

  • Severe psychiatric disorders (e.g. psychosis) that have not been stabilized with e.g., medication (assessed as a part of the clinical process at the clinic). Severe cognitive impairment or language problems (inability to converse for interviews).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

93 participants in 2 patient groups

Treatment as usual (TAU)
No Intervention group
Description:
This control group will receive treatment as usual; conventional counseling
Neurofeedback + TAU
Experimental group
Description:
20 sessions of symptom-based NF training in conjunction with traditional therapy
Treatment:
Behavioral: Neurofeedback

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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