AnxietyNCT04595344
Effects of Listening to Binaural Beats on Anxiety and Pain Scores in Males Undergoing Cystoscopy and Stent Removal
A study testing Listening to Pure Binaural Beats, Listening to classical music and No audio only headphone in people with Anxiety and Cystoscopy, run by Antalya Training and Research Hospital at 1 site in Turkey (Türkiye).
Trial summary
This study aimed to investigate the effects of pure binaural beats on anxiety levels and pain scores using the State-Trait Anxiety Inventory (STAI) questionnaire and Visual Analog Scale (VAS) in male patients undergoing DC and USR procedures under local anesthesia. Read more about this study
- Who is it for?
- Ages 18 years and older, men only
- Conditions the study is for
- Anxiety, Cystoscopy, Pain
- What is being tested?
- Listening to Pure Binaural Beats, Listening to classical music and No audio only headphone
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 352 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 8 Jul 2019to 10 Apr 2020
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- Men only
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Male patient
- negative urine culture
- at least formal schooling (1-8 y of education)
Who cannot join
- hearing or vision problems
- neurological deficits
- mental retardation
- history of chronic pelvic pain syndrome
- history of previous DC or USR procedures
- antidepressant use or analgesia use 24 h before the procedure
- decline to participate
Trial locations and contacts
1 site in 1 country.
Turkey (Türkiye)1 site
Antalya Training and Research Hospital
Antalya
About this study
Official title: Effects of Listening to Binaural Beats on Anxiety Levels and Pain Scores in Male Patients Undergoing Cystoscopy and Ureteral Stent Removal: A Randomized Placebo-controlled Trial
This study aimed to investigate the effects of pure binaural beats on anxiety levels and pain scores using the State-Trait Anxiety Inventory (STAI) questionnaire and Visual Analog Scale (VAS) in male patients undergoing DC and USR procedures under local anesthesia.
Read the detailed description
Diagnostic cystoscopy (DC) and ureteral stent removal (USR) are two common simple procedures in urology practice. DC is generally performed to investigate the etiology of hematuria, recurrent urinary tract infections, lower urinary tract symptoms, and suspected bladder tumor cases.Ureteral stent removal is usually carried out after the placed urethral stent for the treatment of urolithiasis and urethral stricture. In many urology clinics, both procedures are generally performed under local anesthesia. To reduce pain, it is recommended that DC should be performed using a flexible cystoscope. In many urology clinics, USR is performed using a rigid cystoscope in both sexes, as a rigid cystoscope is easier to manipulate during stent removal compared with a flexible cystoscope. Although performed under local anesthesia, both procedures are invasive and can cause increased anxiety levels and pain perception.Anxiety is commonly associated with an increased perception of pain.Therefore, patients who have high anxiety levels experience longer pain and require more analgesics.
Binaural beats have been recommended to reduce anxiety levels and the perception of pain in many treatment modalities.hey were discovered by Dove in 1841 and described in detail by Oster in 1973. Binaural beats are resulted from exposing each ear to two sounds which have steady intensities with different frequencies. A single tone with a midway frequency between the carrier tones is perceived. This frequency also waxes and wanes in amplitudes at a rate equal to the difference between the carrier tones It has been suggested that the human brain alters its dominant wave frequency toward that of the frequency of external stimuli to synchronize neural activity with stimuli from binaural beats.
METHOD
Ethics statement and participant selection
The study was approved by the institutional review board (Approval number and date: 16/15 - 04/07/2019 ). Male patients aged ≥ 18 y with negative urine culture, at least formal schooling (1-8 y of education) who had undergone local DC for various reasons (e.g., hematuria, carcinoma suspicion, follow-up for bladder cancer, and screening of the urethra or prostate) or unilateral USR were included in the study. Informed consent was provided by all the patients who accepted to participate in the study.
The exclusion criteria were patients who had a hearing or vision problems, neurological deficits, mental retardation, a history of chronic pelvic pain syndrome, history of previous DC or USR procedures, antidepressant use, or analgesia use 24 h before the procedure. Patients who underwent a bilateral USR procedure (for USR patients), required additional manipulations of the lower urinary tract (e.g., urethral dilation or biopsies), declined to participate, failed to complete the questionnaires, or could not tolerate the intervention were also excluded from the study.
Randomization, sample size, procedures, interventions, measurement of anxiety levels and pain scores
This was a prospective randomized, non-blinded and placebo-controlled study. After initial exclusions, patients were allocated to the study using the block randomization method. Two main groups were created according to the procedure applied: a DC group (DCG) and a USR group (USRG). The patients in the DCG were divided into three subgroups, according to the intervention applied: DCG-1, patients listened to binaural beats; DCG-2, patients listened to classical music; and DCG-3, patients wore headphones but were not exposed to audio (control group). The USRG was also divided into three subgroups, according to the intervention applied: USRG-1 patients listened to binaural beats; USRG-2 patients listened to classical music; and USRG-3 patients wore headphones but were not exposed to audio (control group). A power analysis indicated a minimum of 62 patients were required in each DCG to have power (1-β) of 0.90 at an alpha value of 0.05, with an effect size of 0.265. A minimum of 41 patients was required in each USRG to have power (1-β) of 0.90 at an alpha value of 0.05 with an effect size of 0.326. The sample sizes of the groups were calculated using the G-power 3.1 (Kiel, Germany).
The STAI is a questionnaire used for measuring anxiety.20 The STAI is often employed to determine an individual's emotional status before surgical interventions. It consists of 20 questions, and STAI scores range from 20 to 80. Higher STAI scores indicate increased anxiety levels. In this study, we used the Turkish validation of the STAI questionnaire to evaluate the patients' anxiety scores.21 Before the DC and USR procedures, the patients who accepted to participate in the study were asked to complete the STAI questionnaire and a nurse recorded the score of each patient (initial STAI: STAI-I). All the patients then put on headphones. For 10 min before the interventions, the patients in DCG-1 and USRG-1 listened to binaural beats, those in DCG-2 and USRG-2 listened to classical music and those in DCG-3 and USRG-3 sat in a quiet room with headphones on but no audio playing. The binaural beats were produced using a software program (Audacity®, version win. 2.3.2, 2019 Audacity Team) at frequency of 10 Hz (a tone of 200 Hz in the right ear and a tone of 210 Hz in the left ear). The binaural beats that the patients in DCG-1 and USRG-1 listened to were "pure" frequencies, with no background music or waves. The classical music that those in DCG-2 and USRG-2 listened to was Mozart's 40th Symphony. The audio headphones used in the DCGs and USRGs were wireless stereo headphones (Sony WH-CH510; Sony Corporation, U.S.). The patients who could not tolerate the interventions were also recorded. After the interventions, the STAI scores of the patients were measured again and recorded. (Terminal STAI: STAI-T). Delta anxiety score is recorded as STAI-I score minus STAI-T score (delta STAI: STAI-D).
The genital area was disinfected with povidone-iodine, and 10 ml of 2% lidocaine jelly was instilled intraurethrally and the penis was clamped approximately 5 min for local anesthesia before the procedures. We used a 17 F video flexible cystoscope for DCG procedure (Hawk GmbH, China) and 17 F rigid cystoscope (Stema GmbH, Germany) with 30 ͦ telescope (Karl Storz GmbH, Germany) for USR procedure. Semi-rigid forceps were used when performing USR. During the DC and USR procedures, the same interventions before the procedures were applied to the patients again. The VAS is a common tool in which patients score their pain level on a scale between 0 and 10.22 In this study, we also used the VAS to evaluate the patients' pain scores. After the procedures, the duration of the procedures and VAS scores 20 of the patients were also recorded. The duration of each procedure was calculated as the time between the entry and exit of the cystoscopy device into the urethral meatus.
Statistical Analysis
The Statistical analysis was made using IBM SPSS Statistics for Windows, Version 25.0 (IBM Corp., Armonk, NY). The assumptions of normality were evaluated by the Shapiro-Wilk test. To determine differences between groups, One-way ANOVA test was used for parametric variables and Kruskal Wallis test was used for non-parametric variables. Bonferroni-Dunn test was used as a post-hoc test for significant cases. Pearson chi-square test and Fisher's exact test were used to compare the categorical variables between the groups while Bonferroni-Dunn test was also used as a post-hoc test for significant cases. A p value of < 0.05 was considered statistically significant.
- Conditions
- Anxiety, Cystoscopy, Pain
- Being tested
- Listening to Pure Binaural Beats, Listening to classical music, No audio only headphone
- Keywords
- Anxiety, Binaural beats, Cystoscopy, Pain, Ureteral Stent Removal
- Medical subject headings
- Anxiety Disorders, Pain
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Listening to Pure Binaural BeatsOther
The patients in DCG ((binaural beat group) ) and USRG (binaural beat group) listened to binaural beats.The binaural beats were produced using a software program (Audacity®, version win. 2.3.2, 2019 Audacity Team) at frequency of 10 Hz (a tone of 200 Hz in the right ear and a tone of 210 Hz in the left ear). The binaural beats that the patients in DCG-1 and USRG-1 listened to were "pure" frequencies, with no background music or waves.
Listening to classical musicOther
The patients in DCG (classical music group) and USRG (classical music group) listened to classical music.The classical music that those in DCG-2 and USRG-2 listened to was Mozart's 40th Symphony.
No audio only headphoneOther
The patients in DCG (placebo group) and USRG (placebo group) sat in a quiet room with headphones on but no audio playing
| Study group | Role | What they receive |
|---|---|---|
| Diagnostic cystoscopy , Binaural beat group | Active comparator | patients listened to binaural beats Receives: Other: Listening to Pure Binaural Beats |
| Diagnostic cystoscopy, Classical music group | Active comparator | patients listened to classical music Receives: Other: Listening to classical music |
| Diagnostic cystoscopy , Placebo group | Placebo comparator | patients no audio only headphones Receives: Other: No audio only headphone |
| Ureteral stent removal, Binaural beat group | Active comparator | patients listened to binaural beats Receives: Other: Listening to Pure Binaural Beats |
| Ureteral stent removal ,Classical music group | Active comparator | patients listened to classical music Receives: Other: Listening to classical music |
| Ureteral stent removal, Placebo group | Placebo comparator | patients no audio only headphones Receives: Other: No audio only headphone |
What is being measured
The primary outcome is the main question the study is designed to answer.
Binaural beats and anxiety levels
Effects of listening to binaural beats on axiety levels before diagnostic cystoscopy and ureteral stent removal procedures. STAI was used to assess the anxiety levels of the patients. STAI scores range from 20 to 80. Higher STAI scores indicate increased anxiety levels
Measured: 10 minutes
Binaural beats and pain scores
Effects of listening to binaural beats on pain scores during diagnostic cystoscopy and ureteral stent removal procedures. VAS vas used to assess the pain scores of patients. The VAS is a common tool in which patients score their pain level on a scale between 0 (no pain) and 10 ( worst pain possible).
Measured: 8 minute
Secondary outcomes (2)
Classical Music and anxiety levels.
Effects of listening to classical music on axiety levels before diagnostic cystoscopy and ureteral stent removal procedures. STAI was used to assess the anxiety levels of the patients.STAI scores range from 20 to 80. Higher STAI scores indicate increased anxiety levels
Measured: 10 minutes
Classical music and pain scores
Effects of listening to classical music on pain scores during diagnostic cystoscopy and ureteral stent removal procedures. VAS vas used to assess the pain scores of patients.he VAS is a common tool in which patients score their pain level on a scale between 0 (no pain) and 10 ( worst pain possible).
Measured: 8 minutes
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 Oct 2020
- Study start8 Jul 2019
- Primary completion26 Mar 2020
- Study completion10 Apr 2020
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for AnxietyStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 352 participants (actual)
Sponsor and investigators
- Lead sponsor
- Antalya Training and Research Hospital
- Sponsor type
- Other government
- Responsible party
- Principal investigator, Mahmut Taha Olcucu, Antalya Training and Research Hospital
- Investigators
- Mahmut Taha MO Ölçücü, Principal investigator, Antalya Training and Research Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04595344
- Sponsor's protocol ID
- 16/15
- Status last verified
- Jul 2021
- First submitted
- 14 Oct 2020
- Last updated
- 28 Jul 2021
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 28 Jul 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effects of Listening to Binaural Beats on Anxiety Levels and Pain Scores in Male Patients Undergoing Cystoscopy and Ureteral Stent Removal: A Randomized Placebo-controlled Trial
- ClinicalTrials.gov ID
- NCT04595344
- Acronym / sponsor ID
- 16/15
- Conditions
- Anxiety, Cystoscopy, Pain
- Keywords
- Anxiety, Binaural beats, Cystoscopy, Pain, Ureteral Stent Removal
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 352 participants (actual)
- Lead sponsor
- Antalya Training and Research HospitalOther government
- Study start
- 8 Jul 2019 (actual)
- Primary completion
- 26 Mar 2020 (actual)
- Study completion
- 10 Apr 2020 (actual)
- First posted
- 20 Oct 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study aimed to investigate the effects of pure binaural beats on anxiety levels and pain scores using the State-Trait Anxiety Inventory (STAI) questionnaire and Visual Analog Scale (VAS) in male patients undergoing DC and USR procedures under local anesthesia.
Detailed description
Diagnostic cystoscopy (DC) and ureteral stent removal (USR) are two common simple procedures in urology practice. DC is generally performed to investigate the etiology of hematuria, recurrent urinary tract infections, lower urinary tract symptoms, and suspected bladder tumor cases.Ureteral stent removal is usually carried out after the placed urethral stent for the treatment of urolithiasis and urethral stricture. In many urology clinics, both procedures are generally performed under local anesthesia. To reduce pain, it is recommended that DC should be performed using a flexible cystoscope. In many urology clinics, USR is performed using a rigid cystoscope in both sexes, as a rigid cystoscope is easier to manipulate during stent removal compared with a flexible cystoscope. Although performed under local anesthesia, both procedures are invasive and can cause increased anxiety levels and pain perception.Anxiety is commonly associated with an increased perception of pain.Therefore, patients who have high anxiety levels experience longer pain and require more analgesics.
Binaural beats have been recommended to reduce anxiety levels and the perception of pain in many treatment modalities.hey were discovered by Dove in 1841 and described in detail by Oster in 1973. Binaural beats are resulted from exposing each ear to two sounds which have steady intensities with different frequencies. A single tone with a midway frequency between the carrier tones is perceived. This frequency also waxes and wanes in amplitudes at a rate equal to the difference between the carrier tones It has been suggested that the human brain alters its dominant wave frequency toward that of the frequency of external stimuli to synchronize neural activity with stimuli from binaural beats.
METHOD
Ethics statement and participant selection
The study was approved by the institutional review board (Approval number and date: 16/15 - 04/07/2019 ). Male patients aged ≥ 18 y with negative urine culture, at least formal schooling (1-8 y of education) who had undergone local DC for various reasons (e.g., hematuria, carcinoma suspicion, follow-up for bladder cancer, and screening of the urethra or prostate) or unilateral USR were included in the study. Informed consent was provided by all the patients who accepted to participate in the study.
The exclusion criteria were patients who had a hearing or vision problems, neurological deficits, mental retardation, a history of chronic pelvic pain syndrome, history of previous DC or USR procedures, antidepressant use, or analgesia use 24 h before the procedure. Patients who underwent a bilateral USR procedure (for USR patients), required additional manipulations of the lower urinary tract (e.g., urethral dilation or biopsies), declined to participate, failed to complete the questionnaires, or could not tolerate the intervention were also excluded from the study.
Randomization, sample size, procedures, interventions, measurement of anxiety levels and pain scores
This was a prospective randomized, non-blinded and placebo-controlled study. After initial exclusions, patients were allocated to the study using the block randomization method. Two main groups were created according to the procedure applied: a DC group (DCG) and a USR group (USRG). The patients in the DCG were divided into three subgroups, according to the intervention applied: DCG-1, patients listened to binaural beats; DCG-2, patients listened to classical music; and DCG-3, patients wore headphones but were not exposed to audio (control group). The USRG was also divided into three subgroups, according to the intervention applied: USRG-1 patients listened to binaural beats; USRG-2 patients listened to classical music; and USRG-3 patients wore headphones but were not exposed to audio (control group). A power analysis indicated a minimum of 62 patients were required in each DCG to have power (1-β) of 0.90 at an alpha value of 0.05, with an effect size of 0.265. A minimum of 41 patients was required in each USRG to have power (1-β) of 0.90 at an alpha value of 0.05 with an effect size of 0.326. The sample sizes of the groups were calculated using the G-power 3.1 (Kiel, Germany).
The STAI is a questionnaire used for measuring anxiety.20 The STAI is often employed to determine an individual's emotional status before surgical interventions. It consists of 20 questions, and STAI scores range from 20 to 80. Higher STAI scores indicate increased anxiety levels. In this study, we used the Turkish validation of the STAI questionnaire to evaluate the patients' anxiety scores.21 Before the DC and USR procedures, the patients who accepted to participate in the study were asked to complete the STAI questionnaire and a nurse recorded the score of each patient (initial STAI: STAI-I). All the patients then put on headphones. For 10 min before the interventions, the patients in DCG-1 and USRG-1 listened to binaural beats, those in DCG-2 and USRG-2 listened to classical music and those in DCG-3 and USRG-3 sat in a quiet room with headphones on but no audio playing. The binaural beats were produced using a software program (Audacity®, version win. 2.3.2, 2019 Audacity Team) at frequency of 10 Hz (a tone of 200 Hz in the right ear and a tone of 210 Hz in the left ear). The binaural beats that the patients in DCG-1 and USRG-1 listened to were "pure" frequencies, with no background music or waves. The classical music that those in DCG-2 and USRG-2 listened to was Mozart's 40th Symphony. The audio headphones used in the DCGs and USRGs were wireless stereo headphones (Sony WH-CH510; Sony Corporation, U.S.). The patients who could not tolerate the interventions were also recorded. After the interventions, the STAI scores of the patients were measured again and recorded. (Terminal STAI: STAI-T). Delta anxiety score is recorded as STAI-I score minus STAI-T score (delta STAI: STAI-D).
The genital area was disinfected with povidone-iodine, and 10 ml of 2% lidocaine jelly was instilled intraurethrally and the penis was clamped approximately 5 min for local anesthesia before the procedures. We used a 17 F video flexible cystoscope for DCG procedure (Hawk GmbH, China) and 17 F rigid cystoscope (Stema GmbH, Germany) with 30 ͦ telescope (Karl Storz GmbH, Germany) for USR procedure. Semi-rigid forceps were used when performing USR. During the DC and USR procedures, the same interventions before the procedures were applied to the patients again. The VAS is a common tool in which patients score their pain level on a scale between 0 and 10.22 In this study, we also used the VAS to evaluate the patients' pain scores. After the procedures, the duration of the procedures and VAS scores 20 of the patients were also recorded. The duration of each procedure was calculated as the time between the entry and exit of the cystoscopy device into the urethral meatus.
Statistical Analysis
The Statistical analysis was made using IBM SPSS Statistics for Windows, Version 25.0 (IBM Corp., Armonk, NY). The assumptions of normality were evaluated by the Shapiro-Wilk test. To determine differences between groups, One-way ANOVA test was used for parametric variables and Kruskal Wallis test was used for non-parametric variables. Bonferroni-Dunn test was used as a post-hoc test for significant cases. Pearson chi-square test and Fisher's exact test were used to compare the categorical variables between the groups while Bonferroni-Dunn test was also used as a post-hoc test for significant cases. A p value of < 0.05 was considered statistically significant.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 6
| Arm | Type | Receives |
|---|---|---|
| Diagnostic cystoscopy , Binaural beat group | Active comparator | Other: Listening to Pure Binaural Beatspatients listened to binaural beats |
| Diagnostic cystoscopy, Classical music group | Active comparator | Other: Listening to classical musicpatients listened to classical music |
| Diagnostic cystoscopy , Placebo group | Placebo comparator | Other: No audio only headphonepatients no audio only headphones |
| Ureteral stent removal, Binaural beat group | Active comparator | Other: Listening to Pure Binaural Beatspatients listened to binaural beats |
| Ureteral stent removal ,Classical music group | Active comparator | Other: Listening to classical musicpatients listened to classical music |
| Ureteral stent removal, Placebo group | Placebo comparator | Other: No audio only headphonepatients no audio only headphones |
Who may qualify
- Ages
- 18 years and older
- Sex
- Male only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- Male patient
- negative urine culture
- at least formal schooling (1-8 y of education)
Key exclusion criteria (7 listed)
- hearing or vision problems
- neurological deficits
- mental retardation
- history of chronic pelvic pain syndrome
- history of previous DC or USR procedures
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Listening to Pure Binaural BeatsThe patients in DCG ((binaural beat group) ) and USRG (binaural beat group) listened to binaural beats.The binaural beats were produced using a software program (Audacity®, version win. 2.3.2, 2019 Audacity Team) at frequency of 10 Hz (a tone of 200 Hz in the right ear and a tone of 210 Hz in the left ear). The binaural beats that the patients in DCG-1 and USRG-1 listened to were "pure" frequencies, with no background music or waves. | Other | Diagnostic cystoscopy , Binaural beat group, Ureteral stent removal, Binaural beat group |
| Listening to classical musicThe patients in DCG (classical music group) and USRG (classical music group) listened to classical music.The classical music that those in DCG-2 and USRG-2 listened to was Mozart's 40th Symphony. | Other | Diagnostic cystoscopy, Classical music group, Ureteral stent removal ,Classical music group |
| No audio only headphoneThe patients in DCG (placebo group) and USRG (placebo group) sat in a quiet room with headphones on but no audio playing | Other | Diagnostic cystoscopy , Placebo group, Ureteral stent removal, Placebo group |
Primary outcome
Binaural beats and anxiety levels
Time frame: 10 minutes
Effects of listening to binaural beats on axiety levels before diagnostic cystoscopy and ureteral stent removal procedures. STAI was used to assess the anxiety levels of the patients. STAI scores range from 20 to 80. Higher STAI scores indicate increased anxiety levels
Binaural beats and pain scores
Time frame: 8 minute
Effects of listening to binaural beats on pain scores during diagnostic cystoscopy and ureteral stent removal procedures. VAS vas used to assess the pain scores of patients. The VAS is a common tool in which patients score their pain level on a scale between 0 (no pain) and 10 ( worst pain possible).
2 secondary outcomes
Classical Music and anxiety levels.
Time frame: 10 minutes
Classical music and pain scores
Time frame: 8 minutes
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Jul 2021.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Mahmut Taha MO Ölçücü principal investigator
Antalya Training and Research Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Listening to Pure Binaural Beats, Listening to classical music and No audio only headphone in people with Anxiety and Cystoscopy, run by Antalya Training and Research Hospital at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 28 Jul 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Binaural beats and anxiety levels (time frame: 10 minutes). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Jul 2021.