Experiences of Psychitherapeutic Outcomes in Women Victims of Domestic ViolenceEPOWVDVNCT06190106
Experiences of Psychotherapeutic Outcomes in Women Victims of Domestic Violence
A study testing Cognitive Behavioral Therapy (Psychotherapeutic Intervention) in people with Experiences of Psychitherapeutic Outcomes in Women Victims of Domestic Violence, run by Government College University Faisalabad at 1 site in Pakistan.
Trial summary
The main objectives of the study are: 1. To explore the experience of undergoing psychotherapy of women victims of domestic violence. 2. To explore the effects of undergoing psychotherapy among women with victims of domestic violence. Read more about this study
- Who is it for?
- Ages 18 to 45 years, women only
- Conditions the study is for
- Experiences of Psychitherapeutic Outcomes in Women Victims of Domestic Violence
- What is being tested?
- Cognitive Behavioral Therapy (Psychotherapeutic Intervention)
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 15 participants
- Where
- 1 sitePakistan
- Study dates
- 15 Nov 2023to 10 Apr 2024
- 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 to 45 years
- Women only
- No healthy volunteers
- Adult
Who may be able to join
- the participants that would be included in the study are females who would be victims of Domestic Violence with the age range of 18 years to 45 years and women who would be eligible for taking psychotherapeutic intervention
Who cannot join
- women with psychotic disorders would be excluded and those who wouldn't meet the criteria of the DASS test
Trial locations and contacts
1 site in 1 country.
About this study
The main objectives of the study are:
- To explore the experience of undergoing psychotherapy of women victims of domestic violence.
- To explore the effects of undergoing psychotherapy among women with victims of domestic violence.
Read the detailed description
Participants:
Purposive sampling techniques would be followed to inquire about the data from the sample. The sample of the present study would be the women who are victims of domestic violence. The study's sample size is 15 which pre and post-testing would be implied. The participants were briefed about the objectives of the present study. Informed consent was taken to ensure the willingness of the participants. First, the DASS test is fulfilled to check out the symptoms caused by domestic violence in women. To fulfill the criteria, they inquired about the topic in detail to get in-depth information from the participants about their experiences and mental health problems caused by domestic violence. Later, they were provided with psychotherapeutic sessions to treat or reduce their mental health problems, and again an in-depth interview about these therapy sessions was conducted to check the effectiveness of the treatment given.
- Being tested
- Cognitive Behavioral Therapy (Psychotherapeutic Intervention)
- Keywords
- Domestic Violence, Psychotherapy, Psychiatric Symptoms, Intimate Partner Victimization (IPV)
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Cognitive Behavioral Therapy (Psychotherapeutic Intervention)Other
A psychotherapeutic intervention CBT is given to assess the improvement and betterment in mental health and to assess the reduction of Psychiatric symptoms like depression, anxiety and stress
| Study group | Role | What they receive |
|---|---|---|
| Experimental treatment group | Experimental | Participants had received 8-10 cognitive behavior therapy-based therapeutic sessions and their feedback was taken to check the positive and negative effects of Psychotherapeutic Intervention (cognitive-behavioral intervention). Receives: Other: Cognitive Behavioral Therapy (Psychotherapeutic Intervention) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Depression anxiety and stress scale
Depression anxiety and stress scale would be used at pre-assessment and post-assessment stage to investigate the impact of ongoing psychotherapy, using qualitative interviews
Measured: 4 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 Jan 2024
- Study start15 Nov 2023
- Primary completion1 Feb 2024 (estimated)
- Study completion10 Apr 2024 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Experiences of Psychitherapeutic Outcomes in Women Victims of Domestic ViolenceStudies 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
- Health services research
- Allocation
- Not applicable
- Intervention model
- Single group
- Model description
- only a single group is studied and their experiences are explored first after screening the psychiatric symptoms of depression, anxiety, and stress and then providing them with Cognitive Behavioral interventions to check the improvement in their Psychiatric symptoms and assess the positive and negative aspects and outcomes of Psychotherapeutic Intervention,
- Masking
- None (open label)
- Enrolment
- 15 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Government College University Faisalabad
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Qasir Abbas, Government College University Faisalabad
- Investigators
- Qasir Abbas, PHD, Principal investigator, Government College University Faisalabad
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06190106
- Sponsor's protocol ID
- GovernmentGCUF
- Acronym
- EPOWVDV
- Status last verified
- Dec 2023
- First submitted
- 19 Dec 2023
- Last updated
- 5 Jan 2024
- 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 5 Jan 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Experiences of Psychotherapeutic Outcomes in Women Victims of Domestic Violence
- ClinicalTrials.gov ID
- NCT06190106
- Acronym / sponsor ID
- EPOWVDV / GovernmentGCUF
- Keywords
- Domestic Violence, Psychotherapy, Psychiatric Symptoms, Intimate Partner Victimization (IPV)
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 15 participants (estimated)
- Lead sponsor
- Government College University FaisalabadUniversity, hospital or other
- Study start
- 15 Nov 2023 (actual)
- Primary completion
- 1 Feb 2024 (estimated)
- Study completion
- 10 Apr 2024 (estimated)
- First posted
- 5 Jan 2024 (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.
The main objectives of the study are:
- To explore the experience of undergoing psychotherapy of women victims of domestic violence.
- To explore the effects of undergoing psychotherapy among women with victims of domestic violence.
Detailed description
Participants:
Purposive sampling techniques would be followed to inquire about the data from the sample. The sample of the present study would be the women who are victims of domestic violence. The study's sample size is 15 which pre and post-testing would be implied. The participants were briefed about the objectives of the present study. Informed consent was taken to ensure the willingness of the participants. First, the DASS test is fulfilled to check out the symptoms caused by domestic violence in women. To fulfill the criteria, they inquired about the topic in detail to get in-depth information from the participants about their experiences and mental health problems caused by domestic violence. Later, they were provided with psychotherapeutic sessions to treat or reduce their mental health problems, and again an in-depth interview about these therapy sessions was conducted to check the effectiveness of the treatment given.
Study design
- Primary purpose
- Health services research
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
- Model description
- only a single group is studied and their experiences are explored first after screening the psychiatric symptoms of depression, anxiety, and stress and then providing them with Cognitive Behavioral interventions to check the improvement in their Psychiatric symptoms and assess the positive and negative aspects and outcomes of Psychotherapeutic Intervention,
| Arm | Type | Receives |
|---|---|---|
| Experimental treatment group | Experimental | Other: Cognitive Behavioral Therapy (Psychotherapeutic Intervention)Participants had received 8-10 cognitive behavior therapy-based therapeutic sessions and their feedback was taken to check the positive and negative effects of Psychotherapeutic Intervention (cognitive-behavioral intervention). |
Who may qualify
- Ages
- 18 to 45 years
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (1 listed)
- the participants that would be included in the study are females who would be victims of Domestic Violence with the age range of 18 years to 45 years and women who would be eligible for taking psychotherapeutic intervention
Key exclusion criteria (1 listed)
- women with psychotic disorders would be excluded and those who wouldn't meet the criteria of the DASS test
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 |
|---|---|---|
| Cognitive Behavioral Therapy (Psychotherapeutic Intervention)A psychotherapeutic intervention CBT is given to assess the improvement and betterment in mental health and to assess the reduction of Psychiatric symptoms like depression, anxiety and stress | Other | Experimental treatment group |
Primary outcome
Depression anxiety and stress scale
Time frame: 4 months
Depression anxiety and stress scale would be used at pre-assessment and post-assessment stage to investigate the impact of ongoing psychotherapy, using qualitative interviews
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 Jan 2024.
- Individual participant dataSharing planned: No
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.
Qasir Abbas, PHD principal investigator
Government College University Faisalabad
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Cognitive Behavioral Therapy (Psychotherapeutic Intervention) in people with Experiences of Psychitherapeutic Outcomes in Women Victims of Domestic Violence, run by Government College University Faisalabad at 1 site in Pakistan.
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 1 inclusion and 1 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: status not confirmed, as of the sponsor's last update on 5 Jan 2024. 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 Pakistan. 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?
Results are not available in the source record.
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?
Depression anxiety and stress scale (time frame: 4 months). 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 5 Jan 2024.