Posttraumatic Stress Symptom

2

Review clinical trials related to Posttraumatic Stress Symptom. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Safe & Sound Protocol in Adults With Trauma and SUD

This study will explore whether the use of the Safe and Sound Protocol (SSP) app is an effective adjunct to treatment as usual (TAU) in individuals with co-occurring substance use disorders and trauma. This study will recruit 129 participants (100 completers) randomized to receive either active or sham SSP in addition to TAU. Participants will utilize the SSP for a minimum of three hours to a maximum of five hours for a total of seven days. Data will be collected at both pre- and post-test. Data to be collected will include measures on affect, anxiety, personality, mindfulness, and posttraumatic stress disorder symptoms. The SSP has shown effectiveness in reducing symptoms of anxiety, depression, and trauma symptoms in pilot studies conducted at other locations. This will be the first study to examine the effectiveness of SSP with individuals with co-occurring SUD and trauma.

Participants needed: 100
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Caron Treatment CentersUpdated: Aug 3, 2026Locations: 1
Eligibility criteria

Ages 18 years old to 75 years old [+5]

Does not speak English [+10]

Status: Recruiting

Voices of Transformation: A Deep Dive Into the Struggles and Successes of Reclaiming Sexuality After Sexual Trauma

This study aims to gain insight into the experiences of participants in the "Take Your Sexuality Back" intervention groups, evaluate the intervention's acceptability, and identify necessary modifications. This study is part of a larger project that seeks to establish a scientific basis for this innovative, group-based treatment to help women who have experienced sexual trauma heal their sexuality. Before implementing the intervention in the healthcare system and initiating a larger randomized controlled trial, the investigators will evaluate the intervention's feasibility and potential efficacy, as well as gain a more comprehensive understanding of treatment outcomes. In addition to collecting quantitative data, it is crucial to gather qualitative data on participants' experiences. In this study, data will be obtained through in-depth interviews with group participants after they complete the intervention.

Participants needed: 20
Trial details
Age: 18-65Biological sex: FemaleType: InterventionalSponsor: Sykehuset TelemarkUpdated: May 4, 2026Locations: 1
Eligibility criteria

A history of sexual trauma [+3]

Acute suicidality [+4]