Butler Hospital
Providence, Rhode Island, 06442, United States
NCT Number: NCT06657950
Phase 1.2: Open Trial N=15 women survivors of interpersonal violence will be enrolled into a single-arm pilot trial to test the adapted integrative hatha yoga and mindful self-compassion program.
Looking for future studies?
Notify Me18 year–65 year
Female
Interventional
Not applicable
Providence, Rhode Island, 06442, United States
In Phase 1.2, the investigators will conduct an open single-arm pilot trial of a 12 week adapted integrative hatha yoga and self-compassion program.
The investigators will enroll 15 women survivors of interpersonal violence in the open pilot trial.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Women who meet criteria for the following:
12 weeks of integrative hatha yoga and mindful self-compassion training
Time frame: Post intervention (month 3)
Feasibility assessed based on number of participants who remained in the intervention (retention).
Time frame: Post intervention (month 3)
The Feasibility of Intervention Measure (FIM) construct comprises four items with each item measured on a 1-5 scale, constituting the score range. Higher scores indicate greater feasibility.
Time frame: Post intervention (month 3)
The Intervention Appropriateness Measure (IAM) construct constitutes four items with each item measured on a 1-5 scale, comprising the total score range. Higher scores indicate greater intervention appropriateness.
Time frame: Post intervention (month 3)
The Acceptability of Intervention Measure (AIM) comprises four items with each item measured on a 1-5 scale, constituting the total score range. Higher scores indicate greater acceptability.
Time frame: Post intervention (month 3)
Satisfaction with treatment assessed with The Client Satisfaction Questionnaire (CSQ-8). The CSQ-8 is an 8-item measure with each item measured on a 1-4 scale, and total score range from 8-32. Higher scores indicate greater client satisfaction.
Time frame: Mid intervention (month 1.5) and Post intervention (month 3)
Participant safety/adverse events will be measured using the SAFTEE. Participants will also be asked weekly if they experienced any injuries as a result of yoga.
Time frame: Post intervention (month 3)
Distress at Month 3. The DASS-21 is a 21-item measure with each item measured on a 0-3 scale, and total score conversion ranging from 0-63. Higher global scores indicate greater psychological distress.
Butler Hospital
Other
Adaptation and Pilot Study of Integrative Yoga and Mindful Self-Compassion (I-YMSC) to Improve Mood in Women Survivors of Interpersonal Violence
Acronym: I-YMSC
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT02970617
Distress, Malignant Neoplasm
Los Angeles, California, United States
View Trial DetailsNCT06960109
Anxiety, Anxiety Disorders
Ankara, Turkey (Türkiye)
View Trial DetailsNCT03078608
Anxiety Disorders, Behavior
Oakland, California, United States
View Trial DetailsNCT04402216
Anxiety, Anxiety Disorders
Aurora, Colorado, United States
View Trial Details