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Comparison of the effectiveness of"ACT"and "CBT"on pain

Comparison of the Effectiveness of Acceptance and Commitment Therapy and Cognitive-Behavioral Therapy on Pain Coping Strategies, Severity of Pain Perception, Disaster Pain Imagery, and Pain Related Anxiety in patients with dental anxiety

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190505043473N2
Enrollment
48
Registered
2020-03-14
Start date
2020-03-01
Completion date
Unknown
Last updated
2020-03-24

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

Conditions

dental anxiety.

Interventions

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to 50 Years

Inclusion criteria

Inclusion criteria: People living in Isfahan age between 19-50 years old higher education level than middle school Willingness to attend intervention sessions and giving written consent minimum physical and cognitive abilities for participating in psychological interventions Supplementary studying of psychiatric criteria using SCL-90-R self-report questionnaire Having the dental anxiety using Stouthard dental anxiety Inventory Having at least 20 natural teeth Additional confirmation of dental anxiety will report by pulse oximeters by a dentist Heart rate of each patient will be measured after relaxing for 5 minutes in the waiting room for 2 times.Then it will be measured twice during the dental treatment, and the mean values will be compared.If the second measure was at least 5 beats per minute higher than the first one, the patient will participate in the study Having at least one treated teeth

Exclusion criteria

Exclusion criteria: systemic diseases or congenital syndromes approved by an internal specialist psychiatric disorders except dental anxiety according to DSM-5 criteria need for emergent dental care approved by a dentist Graduated in any fields of dentistry and psychology receiving psychiatric therapies and chemical drugs in the last six months

Design outcomes

Primary

MeasureTime frame
Pain Coping Strategies score in Coping Strategies Questionnaire. Timepoint: Before intervention, after intervention, after 3 months. Method of measurement: Coping Strategies Questionnaire.;Severity of Pain Perception score by McGill Pain Questionnaire. Timepoint: Before intervention, after intervention, after 3 months. Method of measurement: McGill Pain Questionnaire.;Disaster Pain Imagery score by Pain Catastrophe Scale. Timepoint: Before intervention, after intervention, after 3 months. Method of measurement: Pain Catastrophe Scale.;Pain Related Anxiety score by Pain Anxiety Symptoms Scale. Timepoint: Before intervention, after intervention, after 3 months. Method of measurement: Pain Anxiety Symptoms Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElham sadat Binandeh

Esfahan University of Medical Sciences

binandeh@mail.mui.ac.ir+98 31 3792 5512

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026