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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03351582
Other study ID # DRN 2016/1192/31/1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 15, 2018
Est. completion date December 31, 2019

Study information

Verified date August 2020
Source Ersta Sköndal University College
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The overall purpose of this project is to evaluate the effects of a family therapy intervention for grieving families with children. The main outcome variable is family communication.


Description:

The intervention study will test a supportive family therapy intervention for families where a parent has died from cancer between 2013 and 2015. This will be a randomized controlled trial where participants are assigned to one of three groups using a random number sequence generated by a computer program with approximately 25 families in each intervention group.

Group one will meet with a family therapist for one 90 minute session where the main focus will be on providing information through psychoeducation on grief and communication to participants.

Group two will participate in a family therapy intervention comprised of three 90 minute sessions. participants will receive the same psychoeducation as group one and will also work with the family therapist to enhance family communication and process their grief. The 3 sessions are manual based.

Group three will be the control group and will not meet with a family therapist.

Participants will be asked if their sessions with the family therapist can be tape-recorded, but do not have to consent to this in order to participate. Approximately 6 participants need to be recorded in order to ensure that the family therapists are covering the same topics and giving the same information to all participants. In this way we can ensure that the method of intervention is the same no matter which therapist is delivering the intervention thereby validating the method of intervention.

Follow up will occur 1 month and 6 months after the intervention has ended. Each participant will fill in a short questionnaire regarding grief and Communication. Validated instruments will also be included in the questionnaire.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date December 31, 2019
Est. primary completion date December 31, 2019
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Participants are families with Children ages 3-19 who have completed our questionnaire study and have responses indicating that one or more family members have symptoms of complicated grief or a negative pattern of communication within the family. All family members who live in the same home may participate in the family therapy intervention including new partners or step children. It is up to the family to decide which family members will be included.

Exclusion Criteria:

- Participants must reside in Stockholm, Sweden during data collection, speak and understand written and spoken Swedish.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Grief and Communication Family Intervention
This intervention is an integrative approach which uses techniques from systemic family therapy as well as cognitive behavioral therapy.

Locations

Country Name City State
Sweden Private clinic Stockholm

Sponsors (1)

Lead Sponsor Collaborator
Ersta Sköndal University College

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Parent-Adolescent Communication Scale questionnaire- scores between 20-100 with higher scores indicating better family communication. Change from baseline score at one month, six month, and 18 month follow up
Secondary The Prolonged Grief Disorder Inventory PG-13 questionnaire- scores range between 11-55 higher scores indicate more symptoms of prolonged grief Change from baseline score at one month, six month, and 18 month follow up
Secondary Posttraumatic Stress Disorder Checklist for DSM-5 (PCL-5) questionnaire-The items are rated on a 5-point scale with response descriptors 0 ''not at all'' to 4 ''extremely''. Total scores range from 0 to 80 and a preliminary cut-off score of 33 is suggested as indicating PTSD Change from baseline score at one month, six month, and 18 month follow up
Secondary Montgomery-Åsberg Depression Rating Scale questionnaire-The MADRS was used to assess symptoms of depression. It consists of 9 items. Each item is scored on a 6-point Likert scale. The total score is calculated by summing the answers of the nine items, ranging between 0 and 54 and a higher score indicates a greater risk of depression. Cut off is usually put at 10 for mild depression, 20 for moderate depression and >34 for severe depression Change from baseline score at one month, six month, and 18 month follow up
Secondary The Generalized Anxiety Disorder scale (GAD-7) The GAD-7 was used to assess symptoms of anxiety. It consists of 7 items, scored on a 4-point scale to the response categories from "not at all" to "nearly every day", and adding together the scores for the seven questions. Total scores of 5, 10, and 15 are taken as the cut-off for mild, moderate and severe anxiety, respectively. When used as a screening tool, further evaluation is recommended when the score is 10 or more Change from baseline score at one month, six month, and 18 month follow up
Secondary The Strengths and Difficulties Questionnaire (SDQ) questionnaire- subscale externalizing symptoms scores range from 0-20 with higher scores indicating more internalizing problems. Externalizing subscale scores range from 0-20 with higher scores indicating more externalizing problems. Change from baseline score at one month, six month, and 18 month follow up
Secondary Trauma cognitions checklist Parent report of children's PTSD symptoms. Scores range from 9-27 with higher scores indicating more PTSD symptoms Change from baseline score at one month, six month, and 18 month follow up
Secondary Rosenberg self-esteem scale questionnaire- scores range between 10-40 with higher scores indicating higher self-esteem Change from baseline score at one month, six month, and 18 month follow up
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