Trauma-specific mindfulness-based cognitive therapy for women with post-traumatic stress disorder and a history of domestic abuse: intervention refinement and a randomised feasibility trial (coMforT study).
Lewis NV; Gregory A; Feder GS; Angill-Williams A; Bates S; Glynn J; Halliwell G; Hawcroft C; Kessler D; Lawton M; Leach R; Millband S; Pitt K; Zammit S; Malpass A · Pilot and feasibility studies · 2023 · Randomized feasibility trial
Original publication · Original publication · Original publication
Recorded summary
Feasible with procedural changes; efficacy unresolved.
Recorded limitations
Very small arms; NHS waiting lists weakened control treatment.
Evidence and provenance
Chapter Trust Factor uses a minimum of three distinct qualifying studies. Publication records retain their own evidence and assessment.
Study design and assessment
- design
- Randomized feasibility trial
- assessment
- category
- rct
- is Randomized Controlled Trial
- true
- basis
- Individually randomized parallel-group allocation explicitly described.
- sources
https://pubmed.ncbi.nlm.nih.gov/37400911/ · https://link.springer.com/article/10.1186/s40814-023-01335-w
- review Scope
- full-text
- trust Factor
- scope
- Paper
- status
- assessed
- score
- 2
- randomized Controlled Trial
- true
- peer Reviewed
- true
- blinding
- not-confirmed
- basis
- Individually randomized parallel-group allocation explicitly described.
- sources
https://pubmed.ncbi.nlm.nih.gov/37400911/ · https://link.springer.com/article/10.1186/s40814-023-01335-w
- review Scope
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- human Approval
- false
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- rating Scale
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- jadad
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- score
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- evidence
- evidence Type
- Randomized feasibility trial
- intervention
- Trauma-specific mindfulness-based cognitive therapy Eight group sessions and home practice
- comparator
- Self-referral to NHS psychological treatment
- sample
- 15 TS-MBCT; 5 NHS self-referral control.
- measurement
- Feasibility; PTSD/CPTSD
- timing
- 6 months
- trial Id
- ISRCTN64458065
- relationship Note
- Survivor-focused mind–body intervention. Do not extrapolate to children, perpetrators, or prevention of violence.
- measured Genes
- None recorded
- pathways
- None recorded
- source Access
- level
- full-text
- source URLs
https://pubmed.ncbi.nlm.nih.gov/37400911/ · https://link.springer.com/article/10.1186/s40814-023-01335-w
- retrieved At
- 2026-10-30T07:30:54.246430+00:00
- outcomes
- name
- Feasibility
- result
- 73% uptake; retention among starters 100%; 80% six-month follow-up.
- follow Up
- 6 months
- effect Estimate
- Six of nine progression criteria green; three amber
- uncertainty
- not established from accessed source
- primary Status
- not established from accessed source
- name
- PTSD/CPTSD
- result
- Estimates remained too imprecise to establish efficacy.
- follow Up
- 6 months
- effect Estimate
- Not recorded
- uncertainty
- not established from accessed source
- primary Status
- not established from accessed source
- quality
- risk Of Bias
- Underpowered; nonreceipt of control treatment.
- attrition
- 80% six-month follow-up.
- confounding
- not established from accessed source
- adverse Findings
- Two anxiety-related adverse events; group composition and home body-scan practice raised safety concerns.
- transfer Limits
- Adult women; setting and delivery may limit transfer.
- jadad
- not established
- masking Roles
- participants
- not established from accessed source
- providers
- not established from accessed source
- assessors
- not established from accessed source
- analysts
- not established from accessed source
- population
- relation
- direct
- population
- Adult women survivors
- exposure Evidence
- Explicit intimate partner or domestic violence in eligibility or report.
- rationale
- Survivor-focused mind–body intervention.
- transfer Limit
- Do not extrapolate to children, perpetrators, or prevention of violence.
Topics and recorded topic scores
- key
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- title
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- trust Score
- 2
Citation snapshot and identifiers
- id
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- doi
- 10.1186/s40814-023-01335-w
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- Not recorded
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- retrieved At
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- language
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Complete approved library record
- publication Approval
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- approved-for-publication
- approved By
- Ben Korbel
- approved At
- 2026-11-01
- assessment
- AI assessed; human approved for publication
- scope
- Qualified research-library summaries. No professional clinical peer review or treatment recommendation is claimed.
- source Revision
- audit-r2-42da0a488784
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https://pubmed.ncbi.nlm.nih.gov/37400911/ · https://link.springer.com/article/10.1186/s40814-023-01335-w
- retrieved At
- 2026-10-30T07:30:54.246430+00:00
- editorial Audit
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- claim Check
- Headline finding/design/limitations compared with indexed abstract or accessible primary evidence; retained methods amendments separately adjudicated.
- sources
https://pubmed.ncbi.nlm.nih.gov/37400911/ · https://link.springer.com/article/10.1186/s40814-023-01335-w
- applied Proposals
- None recorded
- method
- AI editorial assessment of all 130 publication records: compare identity, headline finding, design, relevance and limitations with indexed abstracts or available primary material; adjudicate retained source-supported methods amendments. This is a source-limited publication audit, not an independent full-text systematic review or a clinical guideline.
- limitations
Abstract-only records do not establish allocation concealment, complete harms reporting or full risk of bias. · No formal independent RoB 2, GRADE appraisal or numerical reconstruction of every effect was performed. · Source-access labels describe retained appraisal evidence; fuller prior appraisals were checked through their source ledgers and selected material, not independently repeated in full. · Publication counts are not independent trial or participant counts; cohort links and overlapping review evidence remain provisional. · A randomized design cross does not indicate benefit, low risk of bias or human approval. No double-blind trial is verified in this release. · No professional clinical peer review is claimed. Recommended content is limited to accurately qualified research summaries.
- study Family Id
- ISRCTN64458065
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- false
- approaches
mindfulness
- id
- dv-mindbody-37400911
- aliases
- None recorded
- title
- Trauma-specific mindfulness-based cognitive therapy for women with post-traumatic stress disorder and a history of domestic abuse: intervention refinement and a randomised feasibility trial (coMforT study).
- journal
- Pilot and feasibility studies
- neurotransmitters
- None recorded
- year
- 2023
- authors
- Lewis NV; Gregory A; Feder GS; Angill-Williams A; Bates S; Glynn J; Halliwell G; Hawcroft C; Kessler D; Lawton M; Leach R; Millband S; Pitt K; Zammit S; Malpass A
- design
- Randomized feasibility trial
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- Not recorded
- doi
- 10.1186/s40814-023-01335-w
- pmid
- 37400911
- urls
https://doi.org/10.1186/s40814-023-01335-w · https://pubmed.ncbi.nlm.nih.gov/37400911/ · https://link.springer.com/article/10.1186/s40814-023-01335-w
- collections
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Clinical & self-report · Methods & context
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- None recorded
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- summary
- Feasible with procedural changes; efficacy unresolved.
- limitation
- Very small arms; NHS waiting lists weakened control treatment.
- citation Count
- Not recorded
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- study Design Assessment
- category
- rct
- is Randomized Controlled Trial
- true
- basis
- Individually randomized parallel-group allocation explicitly described.
- sources
https://pubmed.ncbi.nlm.nih.gov/37400911/ · https://link.springer.com/article/10.1186/s40814-023-01335-w
- review Scope
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- true
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- Individually randomized parallel-group allocation explicitly described.
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https://pubmed.ncbi.nlm.nih.gov/37400911/ · https://link.springer.com/article/10.1186/s40814-023-01335-w
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- aliases
- None recorded
- title
- Trauma-specific mindfulness-based cognitive therapy for women with post-traumatic stress disorder and a history of domestic abuse: intervention refinement and a randomised feasibility trial (coMforT study).
- authors
- Lewis NV; Gregory A; Feder GS; Angill-Williams A; Bates S; Glynn J; Halliwell G; Hawcroft C; Kessler D; Lawton M; Leach R; Millband S; Pitt K; Zammit S; Malpass A
- year
- 2023
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- Pilot and feasibility studies
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- 10.1186/s40814-023-01335-w
- pmid
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https://doi.org/10.1186/s40814-023-01335-w · https://pubmed.ncbi.nlm.nih.gov/37400911/ · https://link.springer.com/article/10.1186/s40814-023-01335-w
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Clinical & self-report · Methods & context
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ptsd · trauma
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- title
- text
- Trauma-specific mindfulness-based cognitive therapy for women with post-traumatic stress disorder and a history of domestic abuse: intervention refinement and a randomised feasibility trial (coMforT study).
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- Trauma-specific mindfulness-based cognitive therapy for women with post-traumatic stress disorder and a history of domestic abuse: intervention refinement and a randomised feasibility trial (coMforT study).
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adults
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- Adult survivor evidence; no child treatment inference.
- source URL
- https://pubmed.ncbi.nlm.nih.gov/37400911/
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- Feasible with procedural changes; efficacy unresolved.
- summary
- Feasible with procedural changes; efficacy unresolved.
- limitation
- Very small arms; NHS waiting lists weakened control treatment.
- evidence
- evidence Type
- Randomized feasibility trial
- intervention
- Trauma-specific mindfulness-based cognitive therapy Eight group sessions and home practice
- comparator
- Self-referral to NHS psychological treatment
- sample
- 15 TS-MBCT; 5 NHS self-referral control.
- measurement
- Feasibility; PTSD/CPTSD
- timing
- 6 months
- trial Id
- ISRCTN64458065
- relationship Note
- Survivor-focused mind–body intervention. Do not extrapolate to children, perpetrators, or prevention of violence.
- measured Genes
- None recorded
- pathways
- None recorded
- source Access
- level
- full-text
- source URLs
https://pubmed.ncbi.nlm.nih.gov/37400911/ · https://link.springer.com/article/10.1186/s40814-023-01335-w
- retrieved At
- 2026-10-30T07:30:54.246430+00:00
- outcomes
- name
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- follow Up
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- Six of nine progression criteria green; three amber
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- primary Status
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- name
- PTSD/CPTSD
- result
- Estimates remained too imprecise to establish efficacy.
- follow Up
- 6 months
- effect Estimate
- Not recorded
- uncertainty
- not established from accessed source
- primary Status
- not established from accessed source
- quality
- risk Of Bias
- Underpowered; nonreceipt of control treatment.
- attrition
- 80% six-month follow-up.
- confounding
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- adverse Findings
- Two anxiety-related adverse events; group composition and home body-scan practice raised safety concerns.
- transfer Limits
- Adult women; setting and delivery may limit transfer.
- jadad
- not established
- masking Roles
- participants
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- providers
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- assessors
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- analysts
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- population
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- Adult women survivors
- exposure Evidence
- Explicit intimate partner or domestic violence in eligibility or report.
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- sources
https://pubmed.ncbi.nlm.nih.gov/37400911/ · https://link.springer.com/article/10.1186/s40814-023-01335-w
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https://pubmed.ncbi.nlm.nih.gov/37400911/ · https://link.springer.com/article/10.1186/s40814-023-01335-w
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- Ben Korbel
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- assessment
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- scope
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https://pubmed.ncbi.nlm.nih.gov/37400911/ · https://link.springer.com/article/10.1186/s40814-023-01335-w
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- claim Check
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- sources
https://pubmed.ncbi.nlm.nih.gov/37400911/ · https://link.springer.com/article/10.1186/s40814-023-01335-w
- applied Proposals
- None recorded
- method
- AI editorial assessment of all 130 publication records: compare identity, headline finding, design, relevance and limitations with indexed abstracts or available primary material; adjudicate retained source-supported methods amendments. This is a source-limited publication audit, not an independent full-text systematic review or a clinical guideline.
- limitations
Abstract-only records do not establish allocation concealment, complete harms reporting or full risk of bias. · No formal independent RoB 2, GRADE appraisal or numerical reconstruction of every effect was performed. · Source-access labels describe retained appraisal evidence; fuller prior appraisals were checked through their source ledgers and selected material, not independently repeated in full. · Publication counts are not independent trial or participant counts; cohort links and overlapping review evidence remain provisional. · A randomized design cross does not indicate benefit, low risk of bias or human approval. No double-blind trial is verified in this release. · No professional clinical peer review is claimed. Recommended content is limited to accurately qualified research summaries.
- assessment Record
- id
- dv-mindbody-37400911
- title
- Trauma-specific mindfulness-based cognitive therapy for women with post-traumatic stress disorder and a history of domestic abuse: intervention refinement and a randomised feasibility trial (coMforT study).
- authors
Lewis NV · Gregory A · Feder GS · Angill-Williams A · Bates S · Glynn J · Halliwell G · Hawcroft C · Kessler D · Lawton M · Leach R · Millband S · Pitt K · Zammit S · Malpass A
- year
- 2023
- journal
- Pilot and feasibility studies
- doi
- 10.1186/s40814-023-01335-w
- pmid
- 37400911
- trial Registration
ISRCTN64458065
- collection
- language
- intervention Family
- Trauma-specific MBCT
- publication Type
- Primary study
- study Family Id
- ISRCTN64458065
- family Linkage Uncertain
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- None recorded
- relevance
- relation
- direct
- population
- Adult women survivors
- exposure Evidence
- Explicit intimate partner or domestic violence in eligibility or report.
- rationale
- Survivor-focused mind–body intervention.
- transfer Limit
- Do not extrapolate to children, perpetrators, or prevention of violence.
- age
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adult
- reported Range
- not established from accessed source
- youth Scope
- Adult survivor evidence; no child treatment inference.
- country
- United Kingdom
- setting
- Domestic violence and abuse agency
- sample Size
- randomized
- 20
- analyzed
- Not recorded
- description
- 15 TS-MBCT; 5 NHS self-referral control.
- intervention
- description
- Trauma-specific mindfulness-based cognitive therapy
- dose
- Eight group sessions and home practice
- provider
- Trained mindfulness teacher
- comparator
- Self-referral to NHS psychological treatment
- outcomes
- name
- Feasibility
- result
- 73% uptake; retention among starters 100%; 80% six-month follow-up.
- follow Up
- 6 months
- effect Estimate
- Six of nine progression criteria green; three amber
- uncertainty
- not established from accessed source
- primary Status
- not established from accessed source
- name
- PTSD/CPTSD
- result
- Estimates remained too imprecise to establish efficacy.
- follow Up
- 6 months
- effect Estimate
- Not recorded
- uncertainty
- not established from accessed source
- primary Status
- not established from accessed source
- finding
- Feasible with procedural changes; efficacy unresolved.
- limitation
- Very small arms; NHS waiting lists weakened control treatment.
- design
- type
- Randomized feasibility trial
- randomization Evidence
- Individually randomized parallel-group allocation explicitly described.
- masking
- participants
- not established from accessed source
- providers
- not established from accessed source
- assessors
- not established from accessed source
- analysts
- not established from accessed source
- crosses
- 1
- cross Rationale
- Random assignment to comparison groups is explicitly described; double blinding is not verified.
- quality
- risk Of Bias
- Underpowered; nonreceipt of control treatment.
- attrition
- 80% six-month follow-up.
- confounding
- not established from accessed source
- adverse Findings
- Two anxiety-related adverse events; group composition and home body-scan practice raised safety concerns.
- transfer Limits
- Adult women; setting and delivery may limit transfer.
- jadad
- not established
- access
- level
- full-text
- source URLs
https://pubmed.ncbi.nlm.nih.gov/37400911/ · https://link.springer.com/article/10.1186/s40814-023-01335-w
- retrieved At
- 2026-10-30T07:30:54.246430+00:00
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Protocol PMID32161657 and preprint PPR577109 are not additional independent trials.
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- claim Check
- Headline finding/design/limitations compared with indexed abstract or accessible primary evidence; retained methods amendments separately adjudicated.
- sources
https://pubmed.ncbi.nlm.nih.gov/37400911/ · https://link.springer.com/article/10.1186/s40814-023-01335-w
- applied Proposals
- None recorded
- method
- AI editorial assessment of all 130 publication records: compare identity, headline finding, design, relevance and limitations with indexed abstracts or available primary material; adjudicate retained source-supported methods amendments. This is a source-limited publication audit, not an independent full-text systematic review or a clinical guideline.
- limitations
Abstract-only records do not establish allocation concealment, complete harms reporting or full risk of bias. · No formal independent RoB 2, GRADE appraisal or numerical reconstruction of every effect was performed. · Source-access labels describe retained appraisal evidence; fuller prior appraisals were checked through their source ledgers and selected material, not independently repeated in full. · Publication counts are not independent trial or participant counts; cohort links and overlapping review evidence remain provisional. · A randomized design cross does not indicate benefit, low risk of bias or human approval. No double-blind trial is verified in this release. · No professional clinical peer review is claimed. Recommended content is limited to accurately qualified research summaries.
- study Design Assessment
- category
- rct
- is Randomized Controlled Trial
- true
- basis
- Individually randomized parallel-group allocation explicitly described.
- sources
https://pubmed.ncbi.nlm.nih.gov/37400911/ · https://link.springer.com/article/10.1186/s40814-023-01335-w
- review Scope
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- randomized Controlled Trial
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- Random assignment to comparison groups is explicitly described; double blinding is not verified.
- sources
https://pubmed.ncbi.nlm.nih.gov/37400911/ · https://link.springer.com/article/10.1186/s40814-023-01335-w
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- jadad
- status
- unassessed
- score
- Not recorded
- evidence
- population
- relation
- direct
- population
- Adult women survivors
- exposure Evidence
- Explicit intimate partner or domestic violence in eligibility or report.
- rationale
- Survivor-focused mind–body intervention.
- transfer Limit
- Do not extrapolate to children, perpetrators, or prevention of violence.
- intervention
- description
- Trauma-specific mindfulness-based cognitive therapy
- dose
- Eight group sessions and home practice
- provider
- Trained mindfulness teacher
- comparator
- Self-referral to NHS psychological treatment
- outcomes
- name
- Feasibility
- result
- 73% uptake; retention among starters 100%; 80% six-month follow-up.
- follow Up
- 6 months
- effect Estimate
- Six of nine progression criteria green; three amber
- uncertainty
- not established from accessed source
- primary Status
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- name
- PTSD/CPTSD
- result
- Estimates remained too imprecise to establish efficacy.
- follow Up
- 6 months
- effect Estimate
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- source URLs
https://pubmed.ncbi.nlm.nih.gov/37400911/ · https://link.springer.com/article/10.1186/s40814-023-01335-w
- retrieved At
- 2026-10-30T07:30:54.246430+00:00
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- Randomized feasibility trial
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- Trauma-specific mindfulness-based cognitive therapy Eight group sessions and home practice
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- Self-referral to NHS psychological treatment
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- 15 TS-MBCT; 5 NHS self-referral control.
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- Feasibility; PTSD/CPTSD
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- 6 months
- trial Id
- ISRCTN64458065
- relationship Note
- Survivor-focused mind–body intervention. Do not extrapolate to children, perpetrators, or prevention of violence.
- measured Genes
- None recorded
- pathways
- None recorded
- source Access
- level
- full-text
- source URLs
https://pubmed.ncbi.nlm.nih.gov/37400911/ · https://link.springer.com/article/10.1186/s40814-023-01335-w
- retrieved At
- 2026-10-30T07:30:54.246430+00:00
- outcomes
- name
- Feasibility
- result
- 73% uptake; retention among starters 100%; 80% six-month follow-up.
- follow Up
- 6 months
- effect Estimate
- Six of nine progression criteria green; three amber
- uncertainty
- not established from accessed source
- primary Status
- not established from accessed source
- name
- PTSD/CPTSD
- result
- Estimates remained too imprecise to establish efficacy.
- follow Up
- 6 months
- effect Estimate
- Not recorded
- uncertainty
- not established from accessed source
- primary Status
- not established from accessed source
- quality
- risk Of Bias
- Underpowered; nonreceipt of control treatment.
- attrition
- 80% six-month follow-up.
- confounding
- not established from accessed source
- adverse Findings
- Two anxiety-related adverse events; group composition and home body-scan practice raised safety concerns.
- transfer Limits
- Adult women; setting and delivery may limit transfer.
- jadad
- not established
- masking Roles
- participants
- not established from accessed source
- providers
- not established from accessed source
- assessors
- not established from accessed source
- analysts
- not established from accessed source
- population
- relation
- direct
- population
- Adult women survivors
- exposure Evidence
- Explicit intimate partner or domestic violence in eligibility or report.
- rationale
- Survivor-focused mind–body intervention.
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- Do not extrapolate to children, perpetrators, or prevention of violence.
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- unassessed
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- Trauma-specific mindfulness-based cognitive therapy for women with post-traumatic stress disorder and a history of domestic abuse: intervention refinement and a randomised feasibility trial (coMforT study).
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- Trauma-specific mindfulness-based cognitive therapy for women with post-traumatic stress disorder and a history of domestic abuse: intervention refinement and a randomised feasibility trial (coMforT study).
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- post-traumatic
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- Study population or investigated outcome; not a diagnosis or efficacy claim.
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ptsd · trauma
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2
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