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NCT04912414

Brief Family Therapy (BFT) for the Treatment of Psychosomatic Symptoms in Rwanda

Completed NA Last updated 3 June 2021
What this trial tests

NA trial testing Brief Family Therapy (BFT) in Patient Engagement in 120 participants. Completed in 30 December 2020.

Timeline
1 March 2020
Primary endpoint
30 July 2020
30 December 2020

Quick facts

Lead sponsorUniversity of Rwanda
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment120
Start date1 March 2020
Primary completion30 July 2020
Estimated completion30 December 2020
Sites2 locations across Rwanda

Drugs / interventions tested

Conditions studied

Sponsor

University of Rwanda

Who can join

Adults 18 to 59, any sex, with Patient Engagement. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Mental health is fundamental part of the human being worldwide taken as the driver of all daily activities of the people. Psychosomatic disorders are the psychological diseases that are the burden in mental health worldwide. These diseases characterized by the medically unexplained symptomatology (MUS) are considered as a comprehensive, interdisciplinary framework for assessment of psychological factors affecting individual vulnerability, as well as course and outcome of illness; biopsychosocial consideration of patient care in clinical practice; specialist interventions to integrate psychological therapies in the prevention, treatment, and rehabilitation of medical disease. This psychosomatic symptomatology is highly prevalent in developing countries. Prior studies stated that Brief family therapy (BFT) is an effective for MUS. Some possible reasons could be solving conflicts and interpersonal problems by means of training certain skills such as problem solving, developing relationships with others, effective coping, assertiveness and positive thinking. This quasi-experimental design investigates whether BFT can reduce psychosomatic symptoms in Kibungo referral hospital of Eastern Province, Rwanda. Experimental group enroll 60 patients who will be followed up during 2 months. Control group enroll 60 patients. Participants from experimental group will attend 8 sessions of BFT. Statistical analyses will be performed using the SPSS software version 22. As recommended by the declaration of Helsinki, confidentiality and voluntariness were ensured. Informed consents were obtained from the participants. Paired-samples t-test will be used for assessing the means differences between two groups before and after the BFT. 95% of confidence intervals and 5% of statistical significance are applied. In the baseline, sociodemographic questionnaire and psychometric tools will be provided. The psychometric tools will be used in the baseline and at the end of BFT sessions.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Patient Engagement

Currently open trials in the same condition.

Other University of Rwanda trials

Trials by the same sponsor.

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Data sources for this page

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