Therapeutic TouchNCT05922787
The Effect of Reiki on Sexual Function and Sexual Self-Confidence
A study testing Reiki in people with Therapeutic Touch and Sexuality, run by Inonu University at 1 site in Turkey (Türkiye).
Trial summary
Background and Purpose: This study aimed to determine the effect of Reiki on sexual function and sexual self-confidence in women with sexual distress. Materials and Methods: This randomized controlled study was conducted with women between the ages of 15-49 years who were registered at a family health center in the… Read more about this study
- Who is it for?
- Ages 15 to 49 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Therapeutic Touch, Sexuality
- What is being tested?
- Reiki
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 106 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 20 Sep 2022to 1 Jun 2023
- 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 15 to 49 years
- Women only
- Healthy volunteers accepted
- Child, Adult
Who may be able to join
- Being a woman,
- Scoring 11.5 or above on the Female Sexual Distress Scale-Revised (FSDS-R)
- Being sexually active during the study.
Who cannot join
- being pregnant or postpartum
- having a diagnosis of any psychiatric illness or sexual dysfunction
Trial locations and contacts
1 site in 1 country.
About this study
Official title: The Effect of Reiki on Sexual Function and Sexual Self-Confidence in Women With Sexual Distress
Background and Purpose: This study aimed to determine the effect of Reiki on sexual function and sexual self-confidence in women with sexual distress.
Materials and Methods: This randomized controlled study was conducted with women between the ages of 15-49 years who were registered at a family health center in the eastern region of Turkey and had sexual distress. The sample of the study consisted of 106 women, 53 in the experimental group and 53 in the control group. Women in the experimental group received Reiki once a week for four weeks, while no intervention was applied to those in the control group. Data were collected using the Female Sexual Distress Scale-Revised (FSDS-R), the Arizona Sexual Experiences Scale (ASEX), and the Sexual Self-confidence Scale (SSS).
Read the detailed description
- Methods 2.1. Research Design and Sample In this randomized controlled study, participants were randomly assigned to the experimental (Reiki group) or control groups. The study was conducted using women between the ages of 15-49 years who were registered at a Family Health Center in a province of eastern Turkey. This primary healthcare center provides reproductive health services to women such as family planning, education, and counseling, and includes 3 family physicians and 3 family health workers (midwives and/or nurses). The center was randomly selected considering its socioeconomic environment, proximity to the city center, and registered number of women. The center serves approximately 21,000 people, including around 1600 women. Additionally, there is a quiet and peaceful room in the center to hold Reiki sessions. Women who agreed to participate in the study and met the study inclusion criteria were included in the study.
The study inclusion criteria were as follows: being a woman, scoring 11.5 or above on the Female Sexual Distress Scale-Revised (FSDS-R), and being sexually active during the study. The study exclusion criteria were as follows: being pregnant or postpartum, having a diagnosis of any psychiatric illness or sexual dysfunction.
The sample size was determined using OpenEpi (Open Source Epidemiologic Statistics for Public Health) version 3.1, a web-based program. A priori power analysis was performed to estimate the appropriate sample size. As the primary outcome of the study, the mean sexual life score was determined to be 13.70 (with a standard deviation of 5.48) in the literature review. The sample size was calculated as 53 for each group (53 for the experimental group and 53 for the control group) assuming a 5% two-tailed type I error rate, 95% confidence interval, 80% power to represent the population, and a 3-point increase in sexual life score after the intervention.
To reach the sample size, a total of 200 women were evaluated for eligibility criteria. Of them, 47 did not meet the inclusion criteria and 25 refused to participate in the study. In addition, 13 out of 67 women in the experimental group were excluded from the study as they did not continue to participate in Reiki sessions, while 8 out of 61 women in the control group were excluded from the study because they did not want to continue participating in the study. The study was completed with a total of 106 women, 53 in the experimental group and 53 in the control group.
2.2. Randomization Women who agreed to participate in the study and met the inclusion criteria were randomly assigned to experimental and control groups in the order of their arrival at the Family Health Center. A randomization was performed using the Random Integer Generator method, which can be found in the Numbers subsection of the random.org website. Single-column tables were created using numbers from 1 to 106 (https://www.random.org/). Women who referred to the Family Health Center were randomly assigned to numbers 1 and 2 in the column, considering the numbers 1 and 2. The decision of which number would correspond to the experimental or control group was determined by drawing lots. The number 1 was assigned to the experimental group and the number 2 to the control group.
2.3. Data Collection Tools 2.3.1. Personal Information Form The form was created by the researchers and includes questions about women's some introductory characteristics (age, education level, family type, income level, and employment status).
2.3.2. Female Sexual Distress Scale-Revised (FSDS-R) The FSDS-R assesses various aspects of sexual distress in women, including subjective stress and psychological impact associated with sexual dysfunction and is used to identify women with and without sexual dysfunction. The scale consists of 13 items on a five-point Likert scale ranging from never (0) to always. Total scale score ranges between 0 and 52. A higher score indicates higher levels of sexual distress. A cutoff score of ≥11.5 has been recommended to detect the presence of sexually-related personal distress in Turkish women. The Cronbach's alpha reliability coefficient of the scale was found as 0.86 by Aydın et al., while it was determined as 0.78 in this study.
2.3.3. Arizona Sexual Experiences Scale (ASEX) The ASEX assess changes and disorders in sexual function. It was validated in Turkish in 2004. This six-point Likert type scale consists of five items on sexual desire, psychological arousal, physiological arousal (vaginal lubrication), orgasmic capacity, and orgasmic pleasure. Each item is scored from 1 to 6, with a total score ranging from 5 to 30. A lower score indicates a stronger, easier, and more satisfying sexual response, while a higher score suggests sexual dysfunction. The Cronbach's alpha reliability coefficient of the scale was found as 0.89, while it was determined as 0.73 in this study.
2.3.4. Sexual Self-confidences Scale (SSS) The SSS was developed in Turkish by Çelik and validated for its reliability and validity. This four-point Likert type scale consists of 13 items to measure sexual self-confidence. Each item is scored from never (1) to always. Total scale score ranges between 13 and 52. A higher score indicates higher levels of sexual self-confidence. The Cronbach's alpha reliability coefficient of the scale was found as 0.88, while it was determined as 0.78 in this study.
2.4. Data Collection In the study, pre-test data were collected from women through face-to-face interviews in the counseling room at the FHC using a questionnaire that included introductory information as well as the scales used in the study. The same method was used to collect post-test data after four weeks of the intervention. The scales lasted around 10-15 minutes to complete.
2.5. Intervention In the study, women received four Reiki sessions once a week for four weeks from the researchers with Usuı Shiki Ryoho Reiki 1 (Degree 1). The researchers received training and certification in Reiki techniques before starting the intervention. In Reiki 1, the practitioner provides healing through touch or by holding hands a few centimeters above the body, establishing "aura harmony" between the practitioner and the person receiving the treatment. No studies have established what the "energy" referred to in Reiki is; a belief in Reiki is an unsubstantiated belief, rather than an established fact. Reiki practitioners use Reiki with light-hand contact to facilitate an opening of their patients' and their own "energy channels.". Reiki practitioners have explained that the body has seven chakras (at the head, between the eyes, the throat, the chest, the abdominal cavity, the groin, and the upper hip). The sessions were conducted individually in the counseling rooms of the FHC. Each session lasted for 30-40 minutes. The most important rule in Reiki practice for participants is to allow the practitioner to facilitate the flow of energy. It is not necessary for the person receiving Reiki to believe in it because Reiki is universal life energy and is present in everyone. The following sequence is generally applied in Reiki protocols: 1. Before beginning Reiki, the practitioner and the patient remove any jewelry on their bodies. 2. The patient can sit on a chair or lie down on a treatment table with arms and legs open on both sides of the body. 3. It is not necessary to remove the patient's clothes, and their body can be covered with a sheet or a blanket. 4. Reiki is applied by placing hands on the patient's body or holding them a few centimeters above their body. 5. The practitioner sends energy to each chakra or area on the body for 3-5 minutes, depending on the flow of energy, and this time can extend up to 10-20 minutes.6. The practitioner washes their hands. 7. The process is recorded. In addition to the general protocol of Reiki, the practitioner in this study preferred a quiet room and dimmed the lights to prevent distractions. Each woman started the practice lying on her back, fully dressed, with her eyes closed, arms and legs straight and palms facing upwards. At the beginning of the Reiki practice, the practitioner held her hands 2-3 centimeters above each woman's body and made circular movements from her head to her feet to adjust her aura. After this "aura alignment" process, the practitioner placed her hands directly on each woman's body. The practice was performed from top to bottom, starting from the head and spending 3-5 minutes in each hand position at each of the seven main chakras. Each position was held for between one to five minutes, or until the Reiki practitioner felt the energy stop flowing. However, since Reiki application can be done for a longer period on the area where discomfort is felt, and also since the area of sexuality is located in the root chakra, the application of Reiki was ended with a total of 30-40 minutes, with an extra 10 minutes on the root chakra.
No intervention was applied to women in the control group by the researcher; and they only received the service they needed from the FHC.
- Conditions
- Therapeutic Touch, Sexuality
- Being tested
- Reiki
- Keywords
- reiki, sexual distress, sexual self-confidence, sexual experience
- Medical subject headings
- Sexuality
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ReikiOther
In the study, women received four Reiki sessions once a week for four weeks from the researchers with Usuı Shiki Ryoho Reiki 1
| Study group | Role | What they receive |
|---|---|---|
| Experimental | Experimental | Personal Information Form, Female Sexual Distress Scale-Revised (FSD-R),Arizona Sexual Experiences Scale (ASEX),Sexual Self-Confidences Scale (SSS) were utilized for the collection of research data. First of all, FSD-R was applied to the women, and the women who obtained a score above11.5 points or more from the FSD-R were invited to the study.Then, the Personal Information Form, ASEX, and SSS were first applied to the women invited to the study. Women in the experimental group received Reiki once a week for four weeks. No initiative was applied to the pregnant women in the control group. The FSD-R, ASEX and SSS were applied to all participant women after four weeks following the first application. The application of the measurement tools took 10-15 minutes. Receives: Other: Reiki |
| Control | No intervention | The researchers applied no initiative to the control group, and the women in the control group solely had the routine checks. The women in the control group filled out all pretest forms(Personal Information Form, FSD-R, ASEX, SSS. The post-test forms (FSD-R, ASEX, SSS) were re-administered 4 weeks later to women who did not receive any intervention. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Female Sexual Distress Scale-Revised (FSDS-R)
The FSDS-R was assesses various aspects of sexual distress in women, including subjective stress and psychological impact associated with sexual dysfunction and is used to identify women with and without sexual dysfunction. The scale consists of 13 items on a five-point Likert scale ranging from never (0) to always. Total scale score ranges between 0 and 52. A higher score indicates higher levels of sexual distress. A cutoff score of ≥11.5 has been recommended to detect the presence of sexually-related personal distress in Turkish women.
Measured: Change from Sexual Distress at 4 weeks
Secondary outcomes (2)
Arizona Sexual Experiences Scale (ASEX)
The ASEX assess changes and disorders in sexual function. It was validated in Turkish in 2004. This six-point Likert type scale consists of five items on sexual desire, psychological arousal, physiological arousal (vaginal lubrication), orgasmic capacity, and orgasmic pleasure. Each item is scored from 1 to 6, with a total score ranging from 5 to 30. A lower score indicates a stronger, easier, and more satisfying sexual response, while a higher score suggests sexual dysfunction.
Measured: Change from Sexual Experiences at 4 weeks
Sexual Self-confidences Scale (SSS)
This four-point Likert type scale consists of 13 items to measure sexual self-confidence. Each item is scored from never (1) to always. Total scale score ranges between 13 and 52. A higher score indicates higher levels of sexual self-confidence.
Measured: Change from Sexual Self-confidences at 4 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 Jun 2023
- Study start20 Sep 2022
- Primary completion20 Apr 2023
- Study completion1 Jun 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Therapeutic TouchStudies of the same condition, open and under way.
- More trials run by Inonu UniversityThe sponsor's other registered studies.
- 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
- Supportive care
- Allocation
- Randomised
- Intervention model
- Crossover
- Model description
- This study was designed as a randomized controlled trial
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 106 participants (actual)
Sponsor and investigators
- Lead sponsor
- Inonu University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Sümeyye Barut, Inonu University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05922787
- Sponsor's protocol ID
- 2022/3795
- Status last verified
- Jul 2023
- First submitted
- 16 Jun 2023
- Last updated
- 17 Jul 2023
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 17 Jul 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of Reiki on Sexual Function and Sexual Self-Confidence in Women With Sexual Distress
- ClinicalTrials.gov ID
- NCT05922787
- Acronym / sponsor ID
- 2022/3795
- Conditions
- Therapeutic Touch, Sexuality
- Keywords
- reiki, sexual distress, sexual self-confidence, sexual experience
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 106 participants (actual)
- Lead sponsor
- Inonu UniversityUniversity, hospital or other
- Study start
- 20 Sep 2022 (actual)
- Primary completion
- 20 Apr 2023 (actual)
- Study completion
- 1 Jun 2023 (actual)
- First posted
- 28 Jun 2023 (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.
Background and Purpose: This study aimed to determine the effect of Reiki on sexual function and sexual self-confidence in women with sexual distress.
Materials and Methods: This randomized controlled study was conducted with women between the ages of 15-49 years who were registered at a family health center in the eastern region of Turkey and had sexual distress. The sample of the study consisted of 106 women, 53 in the experimental group and 53 in the control group. Women in the experimental group received Reiki once a week for four weeks, while no intervention was applied to those in the control group. Data were collected using the Female Sexual Distress Scale-Revised (FSDS-R), the Arizona Sexual Experiences Scale (ASEX), and the Sexual Self-confidence Scale (SSS).
Detailed description
- Methods 2.1. Research Design and Sample In this randomized controlled study, participants were randomly assigned to the experimental (Reiki group) or control groups. The study was conducted using women between the ages of 15-49 years who were registered at a Family Health Center in a province of eastern Turkey. This primary healthcare center provides reproductive health services to women such as family planning, education, and counseling, and includes 3 family physicians and 3 family health workers (midwives and/or nurses). The center was randomly selected considering its socioeconomic environment, proximity to the city center, and registered number of women. The center serves approximately 21,000 people, including around 1600 women. Additionally, there is a quiet and peaceful room in the center to hold Reiki sessions. Women who agreed to participate in the study and met the study inclusion criteria were included in the study.
The study inclusion criteria were as follows: being a woman, scoring 11.5 or above on the Female Sexual Distress Scale-Revised (FSDS-R), and being sexually active during the study. The study exclusion criteria were as follows: being pregnant or postpartum, having a diagnosis of any psychiatric illness or sexual dysfunction.
The sample size was determined using OpenEpi (Open Source Epidemiologic Statistics for Public Health) version 3.1, a web-based program. A priori power analysis was performed to estimate the appropriate sample size. As the primary outcome of the study, the mean sexual life score was determined to be 13.70 (with a standard deviation of 5.48) in the literature review. The sample size was calculated as 53 for each group (53 for the experimental group and 53 for the control group) assuming a 5% two-tailed type I error rate, 95% confidence interval, 80% power to represent the population, and a 3-point increase in sexual life score after the intervention.
To reach the sample size, a total of 200 women were evaluated for eligibility criteria. Of them, 47 did not meet the inclusion criteria and 25 refused to participate in the study. In addition, 13 out of 67 women in the experimental group were excluded from the study as they did not continue to participate in Reiki sessions, while 8 out of 61 women in the control group were excluded from the study because they did not want to continue participating in the study. The study was completed with a total of 106 women, 53 in the experimental group and 53 in the control group.
2.2. Randomization Women who agreed to participate in the study and met the inclusion criteria were randomly assigned to experimental and control groups in the order of their arrival at the Family Health Center. A randomization was performed using the Random Integer Generator method, which can be found in the Numbers subsection of the random.org website. Single-column tables were created using numbers from 1 to 106 (https://www.random.org/). Women who referred to the Family Health Center were randomly assigned to numbers 1 and 2 in the column, considering the numbers 1 and 2. The decision of which number would correspond to the experimental or control group was determined by drawing lots. The number 1 was assigned to the experimental group and the number 2 to the control group.
2.3. Data Collection Tools 2.3.1. Personal Information Form The form was created by the researchers and includes questions about women's some introductory characteristics (age, education level, family type, income level, and employment status).
2.3.2. Female Sexual Distress Scale-Revised (FSDS-R) The FSDS-R assesses various aspects of sexual distress in women, including subjective stress and psychological impact associated with sexual dysfunction and is used to identify women with and without sexual dysfunction. The scale consists of 13 items on a five-point Likert scale ranging from never (0) to always. Total scale score ranges between 0 and 52. A higher score indicates higher levels of sexual distress. A cutoff score of ≥11.5 has been recommended to detect the presence of sexually-related personal distress in Turkish women. The Cronbach's alpha reliability coefficient of the scale was found as 0.86 by Aydın et al., while it was determined as 0.78 in this study.
2.3.3. Arizona Sexual Experiences Scale (ASEX) The ASEX assess changes and disorders in sexual function. It was validated in Turkish in 2004. This six-point Likert type scale consists of five items on sexual desire, psychological arousal, physiological arousal (vaginal lubrication), orgasmic capacity, and orgasmic pleasure. Each item is scored from 1 to 6, with a total score ranging from 5 to 30. A lower score indicates a stronger, easier, and more satisfying sexual response, while a higher score suggests sexual dysfunction. The Cronbach's alpha reliability coefficient of the scale was found as 0.89, while it was determined as 0.73 in this study.
2.3.4. Sexual Self-confidences Scale (SSS) The SSS was developed in Turkish by Çelik and validated for its reliability and validity. This four-point Likert type scale consists of 13 items to measure sexual self-confidence. Each item is scored from never (1) to always. Total scale score ranges between 13 and 52. A higher score indicates higher levels of sexual self-confidence. The Cronbach's alpha reliability coefficient of the scale was found as 0.88, while it was determined as 0.78 in this study.
2.4. Data Collection In the study, pre-test data were collected from women through face-to-face interviews in the counseling room at the FHC using a questionnaire that included introductory information as well as the scales used in the study. The same method was used to collect post-test data after four weeks of the intervention. The scales lasted around 10-15 minutes to complete.
2.5. Intervention In the study, women received four Reiki sessions once a week for four weeks from the researchers with Usuı Shiki Ryoho Reiki 1 (Degree 1). The researchers received training and certification in Reiki techniques before starting the intervention. In Reiki 1, the practitioner provides healing through touch or by holding hands a few centimeters above the body, establishing "aura harmony" between the practitioner and the person receiving the treatment. No studies have established what the "energy" referred to in Reiki is; a belief in Reiki is an unsubstantiated belief, rather than an established fact. Reiki practitioners use Reiki with light-hand contact to facilitate an opening of their patients' and their own "energy channels.". Reiki practitioners have explained that the body has seven chakras (at the head, between the eyes, the throat, the chest, the abdominal cavity, the groin, and the upper hip). The sessions were conducted individually in the counseling rooms of the FHC. Each session lasted for 30-40 minutes. The most important rule in Reiki practice for participants is to allow the practitioner to facilitate the flow of energy. It is not necessary for the person receiving Reiki to believe in it because Reiki is universal life energy and is present in everyone. The following sequence is generally applied in Reiki protocols: 1. Before beginning Reiki, the practitioner and the patient remove any jewelry on their bodies. 2. The patient can sit on a chair or lie down on a treatment table with arms and legs open on both sides of the body. 3. It is not necessary to remove the patient's clothes, and their body can be covered with a sheet or a blanket. 4. Reiki is applied by placing hands on the patient's body or holding them a few centimeters above their body. 5. The practitioner sends energy to each chakra or area on the body for 3-5 minutes, depending on the flow of energy, and this time can extend up to 10-20 minutes.6. The practitioner washes their hands. 7. The process is recorded. In addition to the general protocol of Reiki, the practitioner in this study preferred a quiet room and dimmed the lights to prevent distractions. Each woman started the practice lying on her back, fully dressed, with her eyes closed, arms and legs straight and palms facing upwards. At the beginning of the Reiki practice, the practitioner held her hands 2-3 centimeters above each woman's body and made circular movements from her head to her feet to adjust her aura. After this "aura alignment" process, the practitioner placed her hands directly on each woman's body. The practice was performed from top to bottom, starting from the head and spending 3-5 minutes in each hand position at each of the seven main chakras. Each position was held for between one to five minutes, or until the Reiki practitioner felt the energy stop flowing. However, since Reiki application can be done for a longer period on the area where discomfort is felt, and also since the area of sexuality is located in the root chakra, the application of Reiki was ended with a total of 30-40 minutes, with an extra 10 minutes on the root chakra.
No intervention was applied to women in the control group by the researcher; and they only received the service they needed from the FHC.
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- Single blind (participant)
- Number of arms
- 2
- Model description
- This study was designed as a randomized controlled trial
| Arm | Type | Receives |
|---|---|---|
| Experimental | Experimental | Other: ReikiPersonal Information Form, Female Sexual Distress Scale-Revised (FSD-R),Arizona Sexual Experiences Scale (ASEX),Sexual Self-Confidences Scale (SSS) were utilized for the collection of research data. First of all, FSD-R was applied to the women, and the women who obtained a score above11.5 points or more from the FSD-R were invited to the study.Then, the Personal Information Form, ASEX, and SSS were first applied to the women invited to the study. Women in the experimental group received Reiki once a week for four weeks. No initiative was applied to the pregnant women in the control group. The FSD-R, ASEX and SSS were applied to all participant women after four weeks following the first application. The application of the measurement tools took 10-15 minutes. |
| Control | No intervention | –The researchers applied no initiative to the control group, and the women in the control group solely had the routine checks. The women in the control group filled out all pretest forms(Personal Information Form, FSD-R, ASEX, SSS. The post-test forms (FSD-R, ASEX, SSS) were re-administered 4 weeks later to women who did not receive any intervention. |
Who may qualify
- Ages
- 15 to 49 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult
Key inclusion criteria (3 listed)
- Being a woman,
- Scoring 11.5 or above on the Female Sexual Distress Scale-Revised (FSDS-R)
- Being sexually active during the study.
Key exclusion criteria (2 listed)
- being pregnant or postpartum
- having a diagnosis of any psychiatric illness or sexual dysfunction
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 |
|---|---|---|
| ReikiIn the study, women received four Reiki sessions once a week for four weeks from the researchers with Usuı Shiki Ryoho Reiki 1 | Other | Experimental |
Primary outcome
Female Sexual Distress Scale-Revised (FSDS-R)
Time frame: Change from Sexual Distress at 4 weeks
The FSDS-R was assesses various aspects of sexual distress in women, including subjective stress and psychological impact associated with sexual dysfunction and is used to identify women with and without sexual dysfunction. The scale consists of 13 items on a five-point Likert scale ranging from never (0) to always. Total scale score ranges between 0 and 52. A higher score indicates higher levels of sexual distress. A cutoff score of ≥11.5 has been recommended to detect the presence of sexually-related personal distress in Turkish women.
2 secondary outcomes
Arizona Sexual Experiences Scale (ASEX)
Time frame: Change from Sexual Experiences at 4 weeks
Sexual Self-confidences Scale (SSS)
Time frame: Change from Sexual Self-confidences at 4 weeks
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 17 Jul 2023.
- Individual participant dataSharing planned: No
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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.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Reiki in people with Therapeutic Touch and Sexuality, run by Inonu University 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 2 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 17 Jul 2023. 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. 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?
Female Sexual Distress Scale-Revised (FSDS-R) (time frame: Change from Sexual Distress at 4 weeks). 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 17 Jul 2023.