A Comparison of Two Psycho-educational Group Interventions for Tinnitus Patients

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT03068871

Enrollment

Registered

2017-03-03

Start date

2017-02-28

Completion date

2017-07-23

Last updated

2018-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tinnitus

Brief summary

participants will be randomized into one of three groups: 3-session CET intervention, 3-session ACT intervention, or Waiting List group. Each weekly session will last up to 2 hours and 10 participants will be assigned to each group. There will be two cohorts, with 30 participants in each cohort. The Waiting List group will receive the CET intervention after the groups have completed theirs.

Interventions

OTHERACT

Psycho-educational group

OTHERCET

Psycho-educational group

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Tinnitus lasting more than 3 months * Hebrew speaking * Use hearing aids if needed * Signed informed consent

Exclusion criteria

* None

Design outcomes

Primary

Measure	Time frame	Description
COPE	Before the intervention (T1) and at the end of intervention (T2-4 weeks after T1), 1 month after end of intervention (T3)	Coping scale questionnaire

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026