Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05852314
Other study ID # CMAP- PND
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date July 10, 2023
Est. completion date June 2024

Study information

Verified date August 2023
Source Pakistan Institute of Living and Learning
Contact Tayyaba Kiran, PhD.
Phone 021-35871845
Email tayyaba.kiran@pill.org.pk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to determine the feasibility and acceptability of culturally adapted CMAP for suicidal Ideation for women in postnatal period. Objectives 1. To adapt existing CMAP Intervention for suicidal ideation (CMAP-SI) in postnatal period. 2. To investigate whether CMAP-SI is feasible and acceptable among women presenting suicidal Ideations in postnatal period; and 3. To test whether there is an indication for the effects of the CMAP in reducing suicidal thoughts among women in postnatal period. 4. To explore participants experiences with CMAP-SI Intervention.


Description:

Suicide is a major public health concern globally, affecting not only the individuals but also family members and society through increased resource costs and productivity loss. Although suicides and suicide attempts occur at a lower rate during pregnancy and the postpartum period than in general population, the prevalence of suicidal thoughts during these periods ranges from 5-14% worldwide and this may result in suicide attempts and completions. There is a growing evidence suggesting that suicidal thoughts and behaviour among women in postnatal period in Low-and Middle-Income Countries (LMICs) are comparable to postnatal women in high resource settings. For instance, in observational studies based on hospital samples of women in postnatal period, 11% women had suicidal behaviour (i.e., thoughts and attempts) in Pakistan, 14% in Ethiopia and 13.6% in Nepal. The causes of these high prevalence rates point to the underlying maternal health issues such as antenatal depression and common mental disorders such as anxiety and depression. Evidence based interventions exists in prevention, care and treatment of suicidal thoughts such as Cognitive Behavioural Therapy (CBT). To deliver a CBT based intervention in Pakistani context, Husain and colleagues tailored a treatment manual: "Life after Self-Harm" to the general population in Pakistan. This Culturally Adapted Manual Assisted Problem solving (CMAP) aims at suicide prevention by reducing the probability of self-harm. Pakistan being a low resource setting faces a huge challenge to provide health care to its population. Therefore, it is important to screen women in postnatal period for risk for suicidal thoughts and behaviour, as well as, the maternal health problems. It is equally important to deliver culturally sensitive interventions which are addressing the psycho-social context wherein suicidal behaviour occurs. Thus, the main aim of this study is to determine the feasibility and acceptability of culturally adapted CMAP for suicidal Ideation for women in postnatal period.


Recruitment information / eligibility

Status Recruiting
Enrollment 90
Est. completion date June 2024
Est. primary completion date June 2024
Accepts healthy volunteers No
Gender Female
Age group 16 Years to 44 Years
Eligibility Inclusion Criteria: 1. 16 to 44-year-old mothers with children 0 - 30 months old 2. Residents of the trial site catchments area 3. Able to provide informed consent 4. Presenting with suicidal Ideation as measured by the Beck Suicidal Ideation Scale (BSSI) as a score <6 (i.e., a score of <6 mean that a patient is not suicidal; see Husain et al., 2014 for further information) and 5. Not requiring in-patient psychiatric treatment. Exclusion Criteria: We will exclude mothers with any physical or psychiatric condition severe enough to prevent study participation.

Study Design


Intervention

Behavioral:
Culturally Adapted Manual Assisted Therapy (CMAP-SI)
C-MAP has been adapted from a self-help guide called Life After Self-Harm based on the principles of CBT. It is a brief problem-solving therapy comprising have 4 sessions weekly and then 4 fortnightly and last about 50 minutes each. The manual has been translated to Urdu giving special consideration to cultural adaptation of phrases and concepts to reflect Pakistani culture. Additionally, culturally appropriate case scenarios were incorporated and a consensual view to addressing cultural factors such as gender role, family conflicts and financial difficulties was taken. The culturally adapted intervention consists of the following components: evaluation of self-harm attempt, crisis skills, problem-solving and CBT techniques to manage emotions, negative thinking, interpersonal relationships, and relapse prevention strategies. Participants will receive sessions according to adapted CMAP-SI manual.

Locations

Country Name City State
Pakistan Benazir Bhutto Hospital Rawalpindi Punjab

Sponsors (1)

Lead Sponsor Collaborator
Pakistan Institute of Living and Learning

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary System Usability Scale Usability of the interventions will be measured with the System Usability Scale (SUS). The SUS is composed of 10 statements that are scored on a 5-point scale of extent of agreement (score 0 to 100). The reliability is good (a=0.91) (Bangor et al., 2008). Interventions with scores of 70 and above are accepted as highly usable (Bangor et al., 2008) and scores between 50 and 70 indicate acceptable usability of an intervention. Interventions with scores 50 and below are subject to concerns about their usability by the target population. At 3 months after baseline
Secondary Beck Scale for Suicidal Ideation (BSS) (Beck et al., 1988) Beck Scale for Suicidal Ideation will be used to measure the reduction in frequency and intensity of suicidal thoughts at baseline and at 3 months. The BSS is a 21-item measure assessing the severity of the suicidal ideation (Beck et al., 1988). Each item is scored from 0 to 2. The total score is obtained by adding the first 19 items and ranges from 0 to 38. High score represents high suicidal ideation. The BSS has good psychometric properties in English (Beck et al., 1988) This scale has been previously used in Pakistan (Husain et al., 2014) and the reported Cronbach's alpha for the Urdu translation of the BSI were 0.75 and 0.89 (Husain et al., 2014) respectively. Baseline and 3 months
Secondary Suicide Attempt and Self-Harm (SASH) (Eylem, 2011) Suicide Attempt and Self-Harm consists of four questions measuring the previous suicide attempt and the presence of self-harm during last 6 weeks with a response on either 'yes, with a frequency of suicide attempt or self harm' or 'no'. SASH questions were taken from the original Self-Harm Questionnaire (Eylem, 2010). The original scale showed good psychometric properties (Eylem, 2010; Ougrin & Boege, 2013). Baseline and 3 months
Secondary Edinburgh postnatal depression scale (EPDS) (Cox et al., 1987) Edinburgh postnatal depression scale will be used to screen depression in mothers with children aged 0-30 months. The maximum score of EPDS is 30, while score 10 or above shows possible depression. The EPDS has been translated into Urdu and validated in Pakistan (Husain et al., 2013). Baseline and 3 months
Secondary Beck Depression Inventory (BDI) (Beck et al., 1961) Beck Depression Inventory will be used to measure symptoms of depression. BDI comprised of 21 items. Each item is scored from 0 to 3. The severity ranges from minimal depressed (score lower than 13) to severely depressed (scores between 29 and 63). It is a reliable and valid measure for assessing depression. The Cronbach's alpha for the Urdu translation of the instrument was 0.96 (Husain et al., 2014). Baseline and 3 months
Secondary Life Events Checklist (Husain et al., 2000) Life events and difficulties will be assessed using a specially designed questionnaire based on our previous work in Pakistan. The domains that accounted for most of the life events and difficulties were included and rated categorically as present or not in the previous 12 months. This questionnaire has been used in a study of postnatal depression in rural Pakistan (Rahman, Iqbal, & Harrington, 2003) and for perinatal depression in Urban Pakistan (Husain et al., 2011). Baseline and 3 months
Secondary Oslo- 3 Social Support Scale (O3SSS) (Dalgard, 2009) Oslo- 3 Social Support Scale will be used to assess the relationship with friends, family and neighbours. Each item is scored on a 5-point rating scale, and the total score ranges from 3 to 15, with high scores indicating a greater level of support. Its structure and reliability have not been well-documented despite its widespread use. The instrument has been validated in Urdu (Husain et al., 2012) and the Cronbach's alpha for the Urdu translation of the instrument was 0.46 (Husain et al., 2021). Baseline and 3 months
Secondary Euro Quol (EQ-5D) (Rabin & Charro, 2001) Euro Quol -5D will be used to measure the health-related quality of life. EQ-5D is an instrument measuring health quality of life and has 5 items: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression (Rabin & Charro, 2001). Each item is required to be rated as 1 (no problem), 2 (some problem) or 3 (extreme problem). The current health state is also rated on a scale ranging from 0 (worst imaginable state) to 100 (best imaginable state). The instrument has been validated in Urdu (Husain et al., 2017). Baseline and 3 months
See also
  Status Clinical Trial Phase
Recruiting NCT04820920 - Online LTP+CaCBT for Treating Depression in British Mothers of African/Caribbean Heritage N/A
Not yet recruiting NCT05148260 - Tackling Postnatal Depression: Culturally Adapted Learning Through Play Plus (LTP+) Intervention for British Mothers of African and Caribbean Origin N/A
Recruiting NCT04834622 - Community Singing Interventions for Postnatal Depression: a Hybrid Type II Effectiveness-implementation Trial N/A
Not yet recruiting NCT04644081 - LTP+CaCBT for Treating Postnatal Depression and Improving Child Wellbeing in Jos Nigeria N/A
Completed NCT06207916 - International Survey of Childbirth-Related Trauma - Swedish Part
Recruiting NCT04332146 - Mindfulness-based Intervention for Postnatal Depression N/A
Active, not recruiting NCT02373709 - Sequence Variations of Genes in the Estrogen Pathway and Perinatal Depression
Not yet recruiting NCT05046405 - Home-based Transcranial Direct Current Stimulation in Postpartum Depression: the Feasibility Study and Pilot Study N/A
Recruiting NCT03346551 - Postnatal Depression, Attachment and Self-defining Memories N/A
Completed NCT01002027 - Three Model Care Pathways for Postnatal Depression N/A
Completed NCT05891717 - Comparative Effect of Training on Postpartum Depression N/A
Completed NCT03499756 - Couple-based Interpersonal Psychotherapy on Postnatal Depression and Family Sense of Coherence N/A
Completed NCT01309516 - Randomised Control Trial of a Complex Intervention for Postnatal Depression Phase 2
Completed NCT04745494 - Studies of Mothers With Postnatal Depression N/A
Completed NCT06301087 - Early Detection Neurodevelopmental Disorders of Children and Prevention of Postnatal Depression by Mobile Health App
Completed NCT00518830 - Treatment of Postnatal Depression for Low-Income Mothers in Primary Care in Santiago, Chile N/A
Recruiting NCT05804708 - Phase 2 Clinical Trial of GH001 in Postpartum Depression Phase 2
Completed NCT03196726 - Behavioural Interventions for Postnatal Depression: a RCT Study N/A
Completed NCT04706442 - Effectiveness of 'Supportive Parenting App' on Parental and Newborn Outcomes N/A
Recruiting NCT05275413 - mHealth Intervention to Reduce Maternal Postnatal Depression and Promote Family Health N/A