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TraumaNCT07589777

Trauma-Informed Yoga Intervention in Young Women

A study testing Trauma-Informed Yoga Intervention Program in people with Trauma and Young Adult Females, run by Saglik Bilimleri Universitesi at 1 site in Turkey (Türkiye).

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The aim of this study is to evaluate the effects of a trauma-informed yoga intervention on psychological trauma symptoms, difficulties in emotion regulation, and interoceptive awareness in young adult women. Read more about this study

Who is it for?
Ages 18 to 25 years, women onlyHealthy volunteers can take part
Conditions the study is for
Trauma, Young Adult Females, Awareness
What is being tested?
Trauma-Informed Yoga Intervention Program
Could I receive a placebo?
No, everyone receives an active treatment
How many people
46 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 Jun 2026to 30 Nov 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

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 to 25 years
  • Women only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Being a woman aged 18-25 years
  • Providing voluntary written informed consent after being informed about the study
  • Scoring within the highest 25th percentile on the Transmitted Psychological Trauma Scale based on the pre-screening assessment, indicating high levels of trauma-related symptoms
  • Having no physical limitations that would prevent participation in weekly sessions and being medically eligible to engage in yoga practices
  • Agreeing to comply with the study protocol, including attendance at intervention sessions and completion of all assessments

Who cannot join

  • Inability to provide reliable responses due to the presence of active psychotic disorder, bipolar disorder, or severe cognitive impairment
  • Being in an acute psychological crisis
  • Initiation of intensive psychotherapy targeting trauma symptoms (e.g., trauma-focused therapy) within the past 3 months or participation in a similar structured psychosocial intervention during the study period
  • Presence of serious musculoskeletal, cardiovascular, or neurological conditions or injuries that would prevent participation in yoga, or medical restriction of physical activity by a physician
  • Having an established regular practice of yoga or meditation

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Duygu Özer, Asst. Prof contact

+905061291978

duyguozer2016@hotmail.com

Turkey (Türkiye)1 site, 1 recruiting
  • Bartın University

    Bartın, Bartın, 74100

    Duygu Özer, duyguozer@bartin.edu.tr

    Recruiting

Other trials in Turkey (Türkiye)

About this study

Official title: Trauma-Informed Yoga Intervention: A Randomized Controlled Trial on Psychological Trauma, Emotion Regulation, and Interoceptive Awareness in Young Adult Women

The aim of this study is to evaluate the effects of a trauma-informed yoga intervention on psychological trauma symptoms, difficulties in emotion regulation, and interoceptive awareness in young adult women.

Read the detailed description

This study will be conducted with young adult women aged 18-25 residing in a selected province. Based on a G*Power analysis, the minimum required sample size was determined to be 46 participants (intervention: n = 23; control: n = 23). Participants will be randomly assigned to the intervention and control groups using a computer-generated simple randomization method (https://www.random.org/integers/

) to ensure unbiased allocation. The intervention group will be implemented in three separate groups, each consisting of 8-10 participants, and will receive the "Trauma-Informed Yoga Intervention Program," which includes eight sessions. Each session will last approximately 45 minutes, and two sessions will be conducted per week for each group. The program will consist of group-based yoga sessions structured in accordance with trauma-informed principles. Pretest and posttest measurements will be used to assess psychological trauma symptoms, difficulties in emotion regulation, and levels of interoceptive awareness among young women.

Being tested
Trauma-Informed Yoga Intervention Program
Keywords
trauma-informed yoga, emotion regulation, interoceptive awareness, psychological trauma, randomized controlled trial
Medical subject headings
Wounds and Injuries, Emotional Regulation, Psychological Trauma

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Trauma-Informed Yoga Intervention ProgramBehavioural

    Intervention program was applied to the intervention group in eight sessions online. Each session will last an average of 45 minutes. There will be two sessions for one group per week. The intervention comprised eight sessions, including establishing a sense of safety and body awareness, listening to the body, integrating emotions and movement, safely engaging with past memories, fostering forgiveness and letting go, strengthening boundaries and personal empowerment, cultivating self-compassion and reconnection, and promoting integration and future orientation.

Study groups in NCT07589777
Study groupRoleWhat they receive
ExperimentalExperimentalParticipants in the intervention group received a trauma-informed, group-based yoga program consisting of eight sessions delivered twice weekly. Each session lasted approximately 45 minutes and was conducted in accordance with trauma-informed principles.
Receives: Behavioral: Trauma-Informed Yoga Intervention Program
ControlNo interventionParticipants in the control group received no structured intervention during the study period and only routine conditions were maintained. Data were collected at the same time points as in the intervention group.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Transmitted Psychological Trauma Scale

    The scale consists of 19 items and three subscales: family functioning (3 items), past family trauma (5 items), and emotion and behavior regulation (11 items). Two items (items 3 and 5) in the scale are reverse scored. Each item is rated on a 5-point Likert scale ranging from 1 (strongly disagree) to 5 (strongly agree). Total scores range from 19 to 95, with higher scores indicating a greater likelihood of transmitted psychological trauma.

    Measured: Baseline, immediately post-intervention, and 1 month post-intervention

Secondary outcomes (2)
  1. Difficulties in Emotion Regulation Scale - Short Form (DERS-16)

    The scale consists of 16 items and five subscales: clarity, goals, impulse, strategies, and non-acceptance. The scale items are rated on a 5-point Likert scale, ranging from 1 (Almost never) to 5 (Almost always), with total scores ranging from 16 to 80. Higher scores indicate greater difficulty in emotion regulation.

    Measured: Baseline, immediately post-intervention, and 1 month post-intervention

  2. Multidimensional Assessment of Interoceptive Awareness - Version 2

    The scale consists of 34 items rated on a 6-point Likert scale ranging from 0 (never) to 5 (always). The number of items varies across the subscales: Noticing, Not-Distracting, Not-Worrying, Attention Regulation, Emotional Awareness, Self-Regulation, Body Listening, and Trusting. Total scores on the scale range from 0 to 170. The scale does not have an established cut-off point. Higher scores indicate greater levels of interoceptive awareness.

    Measured: Baseline, immediately post-intervention, and 1 month post-intervention

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 May 2026
  2. Study start1 Jun 2026
  3. Primary completion30 Sep 2026
  4. Study completion30 Nov 2026 (estimated)

Resources

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
Parallel groups
Model description
Intervention and control group
Masking
Single blind
Who is masked
Participant
Enrolment
46 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07589777
Sponsor's protocol ID
BARU-SBF-DO-3
Status last verified
May 2026
First submitted
2 May 2026
Last updated
2 Nov 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Trauma-Informed Yoga Intervention Program in people with Trauma and Young Adult Females, run by Saglik Bilimleri Universitesi 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 5 inclusion and 5 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: looking for participants now, as of the sponsor's last update on 2 Nov 2026. 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?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Duygu Özer, Asst. Prof (+905061291978, duyguozer2016@hotmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Transmitted Psychological Trauma Scale (time frame: Baseline, immediately post-intervention, and 1 month post-intervention). 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 2 Nov 2026.

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