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Cyclical Sighing for Pain

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Florida State University

Status

Completed

Conditions

Pain

Treatments

Behavioral: Cyclical Sighing
Behavioral: Pain Coping Information

Study type

Interventional

Funder types

Other

Identifiers

NCT06292793
STUDY00004696

Details and patient eligibility

About

This is a single-site, two-arm, parallel-group randomized clinical trial (RCT). The clinical effects of a 4-minute audio-recorded cyclical sighing intervention for orthopedic patients will be investigated relative to a 4-minute audio-recoding about pain psychoeducation.

Enrollment

81 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ≥18
  • Seeking treatment at the Tallahassee Orthopedic Clinic

Exclusion criteria

  • Cognitive impairment preventing completion of study procedures.
  • Other unstable illness judged by medical staff to interfere with study involvement.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

81 participants in 2 patient groups

Pain Coping Information
Active Comparator group
Treatment:
Behavioral: Pain Coping Information
Cyclical Sighing
Experimental group
Treatment:
Behavioral: Cyclical Sighing

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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